A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150623



Internal ID19196325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:25924552..25936853hg38UCSC Ensembl
OuterchrY:28070699..28083000hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3812302
hg1912302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996097
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150623
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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