A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002073



Internal ID19188036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56821552..56887953hg38UCSC Ensembl
OuterchrY:58967699..59034100hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3866402
hg1966402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151136
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002073
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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