A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005983



Internal ID71600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156901454..156907390hg38UCSC Ensembl
chr7:156694148..156700084hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385937
hg195937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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