A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375785



Internal ID22125676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44336152..44336878hg38UCSC Ensembl
chr15:44628350..44629076hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220602
Supporting Variants
SamplesHG00512
Known GenesCASC4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375785
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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