A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622262



Internal ID7009121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6995467..7032241hg38UCSC Ensembl
Innerchr10:6995467..7032241hg38UCSC Ensembl
Outerchr10:6994967..7032741hg38UCSC Ensembl
chr10:7037429..7074203hg19UCSC Ensembl
Innerchr10:7037429..7074203hg19UCSC Ensembl
Outerchr10:7036929..7074703hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3836775
hg1936775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13688342
SamplesNA19758
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622262
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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