A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153299



Internal ID19201145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:281032..314633hg38UCSC Ensembl
OuterchrY:147699..181300hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3833602
hg1933602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001218
SamplesKWB1
Known GenesGTPBP6, PLCXD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153299
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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