A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622976



Internal ID7009833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38095589..38112908hg38UCSC Ensembl
Innerchr10:38096089..38112408hg38UCSC Ensembl
Outerchr10:38094589..38113908hg38UCSC Ensembl
chr10:38384517..38401836hg19UCSC Ensembl
Innerchr10:38385017..38401336hg19UCSC Ensembl
Outerchr10:38383517..38402836hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3817320
hg1917320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13757266
SamplesHG02407
Known GenesZNF37A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622976
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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