A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001092



Internal ID68317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75452779..75459889hg38UCSC Ensembl
chr7:75082052..75089154hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387111
hg197103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142347
Supporting Variants
Samples
Known GenesPOM121C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001092
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.160094


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