A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13685662



Internal ID3687478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5771963..5772724hg38UCSC Ensembl
Innerchr10:5772013..5772674hg38UCSC Ensembl
Outerchr10:5771909..5772778hg38UCSC Ensembl
chr10:5813926..5814687hg19UCSC Ensembl
Innerchr10:5813976..5814637hg19UCSC Ensembl
Outerchr10:5813872..5814741hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622233
Supporting Variants
SamplesHG03777
Known GenesGDI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13685662
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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