A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151085



Internal ID19201872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9860690..9872291hg38UCSC Ensembl
OuterchrY:9698299..9709900hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3811602
hg1911602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002020
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151085
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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