A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148201



Internal ID19197520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:23662952..23678453hg38UCSC Ensembl
OuterchrY:25809099..25824600hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3815502
hg1915502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001714
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148201
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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