A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998059



Internal ID18810909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241830506..242001132hg38UCSC Ensembl
Innerchr2:242772683..242943283hg19UCSC Ensembl
Innerchr2:242421356..242591956hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38170627
hg19170601
hg18170601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3587009
Samples
Known GenesCXXC11, PDCD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998059
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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