A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13764061



Internal ID3765877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42584089..42655641hg38UCSC Ensembl
chr10:43079537..43151089hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3871553
hg1971553
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623017
Supporting Variants
SamplesNA18620
Known GenesZNF33B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13764061
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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