A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150952



Internal ID19200466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24251452..24264053hg38UCSC Ensembl
OuterchrY:26397599..26410200hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3812602
hg1912602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001887
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150952
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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