A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009502



Internal ID19098720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66527233..66611140hg38UCSC Ensembl
Innerchr4:67392951..67476858hg19UCSC Ensembl
Innerchr4:67075546..67159453hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3883908
hg1983908
hg1883908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626064, nssv3626063
Samples
Known GenesMIR548AJ2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009502
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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