A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029796



Internal ID87572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138177536..138223536hg38UCSC Ensembl
chr9:141071988..141113986hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3846001
hg1941999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141845
Supporting Variants
Samples
Known GenesFAM157B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029796
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.036044


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