A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622604



Internal ID7009462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22882909..22889277hg38UCSC Ensembl
Innerchr10:22883409..22888777hg38UCSC Ensembl
Outerchr10:22881909..22890277hg38UCSC Ensembl
chr10:23171838..23178206hg19UCSC Ensembl
Innerchr10:23172338..23177706hg19UCSC Ensembl
Outerchr10:23170838..23179206hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg386369
hg196369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13716071
SamplesHG03900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622604
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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