A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012915



Internal ID19102132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49050193..49295206hg38UCSC Ensembl
Innerchr4:49052210..49297223hg19UCSC Ensembl
Innerchr4:48746967..48991980hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38245014
hg19245014
hg18245014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5204n100
Supporting Variantsnssv3625142
Samples
Known GenesCWH43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012915
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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