A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007598



Internal ID19096817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:32242139..32301077hg38UCSC Ensembl
Innerchr4:32243761..32302699hg19UCSC Ensembl
Innerchr4:31887659..31946597hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3858939
hg1958939
hg1858939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620641
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)nsv1007598
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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