A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132809



Internal ID19254701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11085224..11124924hg38UCSC Ensembl
OuterchrY:13240900..13280600hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3839701
hg1939701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987601
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132809
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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