A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977971



Internal ID19236418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:57205549..57209649hg38UCSC Ensembl
OuterchrY:59351700..59355800hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125166
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977971
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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