A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695944



Internal ID119610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59559541..59560183hg38UCSC Ensembl
chr14:60026259..60026901hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503246
Supporting Variants
Samples
Known GenesCCDC175
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695944
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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