A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005307



Internal ID71163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154822756..154824935hg38UCSC Ensembl
chr7:154614466..154616645hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382180
hg192180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479442
Supporting Variants
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005307
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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