A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953118



Internal ID17301992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56673271..56771470hg38UCSC Ensembl
OuterchrY:58819401..58917600hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3898200
hg1998200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000406
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953118
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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