A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006871



Internal ID72197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156148105..156152912hg38UCSC Ensembl
chr7:155940799..155945606hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384808
hg194808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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