A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380102



Internal ID22266659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39930278..39930709hg38UCSC Ensembl
chr17:38086531..38086962hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228258
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380102
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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