A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987608



Internal ID19215988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26638053..26672953hg38UCSC Ensembl
OuterchrY:28784200..28819100hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3834901
hg1934901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132816
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987608
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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