A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023394



Internal ID19112611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:63473094..63687026hg38UCSC Ensembl
Innerchr7:62933472..63147404hg19UCSC Ensembl
Innerchr7:62570907..62784839hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38213933
hg19213933
hg18213933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661965
Samples
Known GenesMIR4283-1, MIR4283-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023394
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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