A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009681



Internal ID19098899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57185470..57232450hg38UCSC Ensembl
Innerchr4:58051636..58098616hg19UCSC Ensembl
Innerchr4:57746393..57793373hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3846981
hg1946981
hg1846981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5217n100
Supporting Variantsnssv3625309, nssv3625308, nssv3625310, nssv3739454
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)nsv1009681
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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