A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388938



Internal ID22256827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63732270..63732834hg38UCSC Ensembl
chr17:61809630..61810194hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222598
Supporting Variants
SamplesNA19238
Known GenesSTRADA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388938
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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