A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055802



Internal ID105034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9283525..9300825hg38UCSC Ensembl
chr12:9436121..9453421hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3817301
hg1917301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143317
Supporting Variants
Samples
Known GenesLOC642846
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055802
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009641


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