A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153990



Internal ID19196499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:17620719..17633120hg38UCSC Ensembl
OuterchrY:19732599..19745000hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3812402
hg1912402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003266
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153990
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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