A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005077



Internal ID19094294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:198062049..198111695hg38UCSC Ensembl
Innerchr3:197788920..197838566hg19UCSC Ensembl
Innerchr3:199273317..199322963hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3849647
hg1949647
hg1849647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5047n100
Supporting Variantsnssv3617041
Samples
Known GenesANKRD18DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005077
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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