A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151433



Internal ID19195529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26637952..26673053hg38UCSC Ensembl
OuterchrY:28784099..28819200hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3835102
hg1935102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003996
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151433
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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