A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119395



Internal ID19261400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56821553..56887153hg38UCSC Ensembl
OuterchrY:58967700..59033300hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3865601
hg1965601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959837
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119395
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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