A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031122



Internal ID19120343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164248994..164349933hg38UCSC Ensembl
Innerchr4:165170146..165271085hg19UCSC Ensembl
Innerchr4:165389596..165490535hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38100940
hg19100940
hg18100940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5460n100
Supporting Variantsnssv3634167
Samples
Known GenesMARCH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031122
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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