A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010600



Internal ID19099817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:223417333..223487357hg38UCSC Ensembl
Innerchr2:224282051..224352075hg19UCSC Ensembl
Innerchr2:223990295..224060319hg18UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3870025
hg1970025
hg1870025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586825
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010600
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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