A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980122



Internal ID19231119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11295515..11296578hg38UCSC Ensembl
OuterchrY:13451191..13452254hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117920
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980122
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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