A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14391502



Internal ID22270175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44388135..44388776hg38UCSC Ensembl
chr15:44680333..44680974hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224377
Supporting Variants
SamplesNA19239
Known GenesCASC4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14391502
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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