A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140088



Internal ID19248350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:864965..933565hg38UCSC Ensembl
OuterchrY:775700..844300hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3868601
hg1968601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978424
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140088
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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