A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110653



Internal ID18908857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24209353..24214853hg38UCSC Ensembl
OuterchrY:26355500..26361000hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960308
SamplesKWS1
Known GenesGOLGA2P2Y, GOLGA2P3Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110653
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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