A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999656



Internal ID19191577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:19936713..19950414hg38UCSC Ensembl
OuterchrY:22098599..22112300hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3813702
hg1913702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1152469
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999656
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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