A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011854



Internal ID19101072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57189069..57237378hg38UCSC Ensembl
Innerchr4:58055235..58103544hg19UCSC Ensembl
Innerchr4:57749992..57798301hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3848310
hg1948310
hg1848310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5217n100
Supporting Variantsnssv3626500
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)nsv1011854
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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