A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005669



Internal ID71393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149053812..149054090hg38UCSC Ensembl
chr7:148750904..148751182hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485026
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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