A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149113



Internal ID19201369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:5606458..5612659hg38UCSC Ensembl
OuterchrY:5474499..5480700hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg386202
hg196202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002624
SamplesKWB1
Known GenesPCDH11Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149113
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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