A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996882



Internal ID19192118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10626585..10633440hg38UCSC Ensembl
OuterchrY:13137099..13144000hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg386856
hg196902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152273
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996882
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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