A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863963



Internal ID3865779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75223245..75223895hg38UCSC Ensembl
Innerchr10:75223246..75223894hg38UCSC Ensembl
Outerchr10:75223244..75223896hg38UCSC Ensembl
chr10:76983003..76983653hg19UCSC Ensembl
Innerchr10:76983004..76983652hg19UCSC Ensembl
Outerchr10:76983002..76983654hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623848
Supporting Variants
SamplesHG03911
Known GenesVDAC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863963
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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