A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014721



Internal ID19103938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44948206..44997590hg38UCSC Ensembl
Innerchr4:44950223..44999607hg19UCSC Ensembl
Innerchr4:44644980..44694364hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3849385
hg1949385
hg1849385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5198n100
Supporting Variantsnssv3625055
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014721
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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