A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000353



Internal ID17293305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10134292..10162491hg38UCSC Ensembl
OuterchrY:9971901..10000100hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3828200
hg1928200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953740
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000353
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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