A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6249685



Internal ID9066377
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 Flag1
Merged StatusS
Merged Variantsesv2666356
Supporting Variants
SamplesHG00734
Known GenesGPR50
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6249685
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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