A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377075



Internal ID22268866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42350281..42350807hg38UCSC Ensembl
chr15:42642479..42643005hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228186
Supporting Variants
SamplesNA19238
Known GenesGANC
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377075
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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