A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066969



Internal ID19156188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2603007..2644986hg38UCSC Ensembl
Innerchr18:2603006..2644985hg19UCSC Ensembl
Innerchr18:2593006..2634985hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3841980
hg1941980
hg1841980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564062
Samples
Known GenesNDC80
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066969
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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