A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005931



Internal ID71569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155642651..155643401hg38UCSC Ensembl
chr7:155435345..155436095hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005931
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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