A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626064



Internal ID18924345
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 StatusS
Merged Variantsnsv1009502
Supporting Variants
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)nssv3626064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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