A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008121



Internal ID19097340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:67061988..67224979hg38UCSC Ensembl
Innerchr4:67927706..68090697hg19UCSC Ensembl
Innerchr4:67610301..67773292hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38162992
hg19162992
hg18162992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3740197
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)nsv1008121
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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