A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003993



Internal ID19188439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:1641306..1642807hg38UCSC Ensembl
OuterchrY:1710199..1711700hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151428
Supporting Variants
SamplesKWB1
Known GenesASMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003993
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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