A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002456



Internal ID19190013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:429964..439365hg38UCSC Ensembl
OuterchrY:340699..350100hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg389402
hg199402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153802
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002456
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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