A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013620



Internal ID19102839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57187577..57234405hg38UCSC Ensembl
Innerchr4:58053743..58100571hg19UCSC Ensembl
Innerchr4:57748500..57795328hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3846829
hg1946829
hg1846829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5217n100
Supporting Variantsnssv3739487
Samples
Known GenesIGFBP7-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013620
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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