A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987609



Internal ID19219362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56673271..56771471hg38UCSC Ensembl
OuterchrY:58819400..58917600hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3898201
hg1998201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115948
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987609
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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