A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963515



Internal ID19225425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56831584..56836805hg38UCSC Ensembl
OuterchrY:58977731..58982952hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg385222
hg195222
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111400
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963515
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer