A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140083



Internal ID19280138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24400..44500hg38UCSC Ensembl
OuterchrY:24400..44500hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3820101
hg1920101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4327n106
Supporting Variantsnssv3978419
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140083
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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