A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980586



Internal ID54440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37712970..37917713hg38UCSC Ensembl
chr6:37680746..37885489hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38204744
hg19204744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473793
Supporting Variants
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980586
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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