A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622975



Internal ID7009832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38042306..38044799hg38UCSC Ensembl
Innerchr10:38042349..38044757hg38UCSC Ensembl
Outerchr10:38042264..38044842hg38UCSC Ensembl
chr10:38331234..38333727hg19UCSC Ensembl
Innerchr10:38331277..38333685hg19UCSC Ensembl
Outerchr10:38331192..38333770hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg382494
hg192494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13757265
SamplesHG02652
Known GenesZNF33A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622975
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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