A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005914



Internal ID71558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154058237..154058410hg38UCSC Ensembl
chr7:153755322..153755495hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477608
Supporting Variants
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005914
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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