A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440617



Internal ID21098170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122096546..122097191hg38UCSC Ensembl
chr10:123856061..123856706hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978198
Samples
Known GenesTACC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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