A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666356



Internal ID9932461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151174844..151179350hg38UCSC Ensembl
OuterchrX:151174473..151179720hg38UCSC Ensembl
InnerchrX:150343316..150347822hg19UCSC Ensembl
OuterchrX:150342945..150348192hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385248
hg195248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1406e199
Supporting Variantsessv5814562, essv5770810, essv5581443, essv6249685, essv5476753, essv5953746, essv6267157, essv6276956, essv6584226, essv6009285, essv5658046, essv5838066, essv5591067, essv5590866, essv5449655, essv6091515, essv5854911, essv5930733, essv6072281, essv6435163, essv6065780, essv5711399, essv6198507, essv5826713, essv6536282, essv5598719, essv5746586, essv5636635, essv6549223, essv5740459, essv6534220, essv5459751, essv6307437, essv5635057, essv5781522, essv6323378, essv5824962, essv5751917
SamplesHG01060, HG01173, HG01052, HG01079, HG01188, HG01066, HG00640, HG00737, HG01051, HG00641, HG01167, HG00736, HG01069, HG01170, HG01072, HG01176, HG00637, HG01048, HG00731, HG01187, HG00732, HG00740, HG01047, HG01102, HG01197, HG01182, HG01101, HG01107, HG01204, HG01075, HG01190, HG00734, HG00638, HG01108, HG01082, HG01097, HG01061, HG00553
Known GenesGPR50
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666356
Frequency
Sample Size1151
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer