A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701603



Internal ID125269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44411579..44412740hg38UCSC Ensembl
chr15:44703777..44704938hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522636
Supporting Variants
Samples
Known GenesCASC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701603
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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