A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012689



Internal ID19101906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61457429..61639700hg38UCSC Ensembl
Innerchr2:61684564..61866835hg19UCSC Ensembl
Innerchr2:61538068..61720339hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38182272
hg19182272
hg18182272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577248
Samples
Known GenesUSP34, XPO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012689
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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