A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001653



Internal ID19187268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10594085..10621386hg38UCSC Ensembl
OuterchrY:13104599..13131900hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3827302
hg1927302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148142
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001653
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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