A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013766



Internal ID19102985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:238489360..238612525hg38UCSC Ensembl
Innerchr1:238652660..238775825hg19UCSC Ensembl
Innerchr1:236719283..236842448hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38123166
hg19123166
hg18123166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv593n100
Supporting Variantsnssv3495199
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)nsv1013766
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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