A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000409



Internal ID19089626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62781408..62813912hg38UCSC Ensembl
Innerchr4:63647126..63679630hg19UCSC Ensembl
Innerchr4:63329721..63362225hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3832505
hg1932505
hg1832505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739501, nssv3626527, nssv3739502
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)nsv1000409
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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