A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001021



Internal ID68254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74854779..74960779hg38UCSC Ensembl
chr7:74271070..74375488hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38106001
hg19104419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141718
Supporting Variants
Samples
Known GenesPMS2P5, STAG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001021
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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