A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714005



Internal ID137671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63559157..63559360hg38UCSC Ensembl
chr17:61636518..61636721hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528708
Supporting Variants
Samples
Known GenesDCAF7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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