A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014926



Internal ID18757461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112574087..112770975hg38UCSC Ensembl
Innerchr4:113495243..113692131hg19UCSC Ensembl
Innerchr4:113714692..113911580hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38196889
hg19196889
hg18196889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632704
Samples
Known GenesC4orf21, LARP7, MIR302A, MIR302B, MIR302C, MIR302D, MIR367
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014926
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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