A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980584



Internal ID54439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35041209..35043826hg38UCSC Ensembl
chr6:35008986..35011603hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382618
hg192618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455658
Supporting Variants
Samples
Known GenesANKS1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980584
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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