A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119393



Internal ID19264166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24270253..24287153hg38UCSC Ensembl
OuterchrY:26416400..26433300hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3816901
hg1916901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959835
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119393
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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