A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014606



Internal ID19103824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:12878207..13026244hg38UCSC Ensembl
Innerchr2:13018333..13166369hg19UCSC Ensembl
Innerchr2:12935784..13083820hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38148038
hg19148037
hg18148037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3717n100
Supporting Variantsnssv3576970
Samples
Known GenesLOC100506474
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014606
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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