A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004831



Internal ID70853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149554010..149556545hg38UCSC Ensembl
chr7:149251101..149253636hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382536
hg192536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480085
Supporting Variants
Samples
Known GenesZNF767
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004831
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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