A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999077



Internal ID19194353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:25473952..25489453hg38UCSC Ensembl
OuterchrY:27620099..27635600hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3815502
hg1915502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151893
Supporting Variants
SamplesKWB1
Known GenesCSPG4P1Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999077
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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