A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004777



Internal ID70823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149079860..149113802hg38UCSC Ensembl
chr7:148776952..148810894hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3833943
hg1933943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488436
Supporting Variants
Samples
Known GenesZNF425, ZNF786
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004777
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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