A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976357



Internal ID19236288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10168706..10168767hg38UCSC Ensembl
OuterchrY:10006315..10006376hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115308
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976357
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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