A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997432



Internal ID19156968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:111437049..111474793hg38UCSC Ensembl
Innerchr4:112358205..112395949hg19UCSC Ensembl
Innerchr4:112577654..112615398hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3837745
hg1937745
hg1837745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632703
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)nsv997432
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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