A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438827



Internal ID21096380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43633465..43640234hg38UCSC Ensembl
chr10:44128913..44135682hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386770
hg196770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182748
Samples
Known GenesZNF32-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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