A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960299



Internal ID19216218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11460724..11592824hg38UCSC Ensembl
OuterchrY:13616400..13748500hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38132101
hg19132101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110644
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960299
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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