A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151136



Internal ID19198449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56821552..56887953hg38UCSC Ensembl
OuterchrY:58967699..59034100hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3866402
hg1966402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002073
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151136
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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