A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663043



Internal ID9929148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23765526..23771282hg38UCSC Ensembl
Outerchr1:23765155..23771652hg38UCSC Ensembl
Innerchr1:24092016..24097772hg19UCSC Ensembl
Outerchr1:24091645..24098142hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386498
hg196498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv29e199
Supporting Variantsessv5529218, essv5785705, essv5574355, essv5556482, essv6443940, essv6350324, essv5802849, essv5977582, essv5786243, essv5728551, essv6157927, essv6531162, essv5922250, essv6020449, essv5993592
SamplesNA19350, NA19393, NA19443, NA19446, NA19448, NA19383, NA19452, NA19469, NA19436, NA19440, NA19470, NA19438, NA19468, NA19430, NA19431
Known GenesLOC100506963
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663043
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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