A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012666



Internal ID19101883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..51522hg38UCSC Ensembl
Innerchr4:12269..51416hg19UCSC Ensembl
Innerchr4:2269..41416hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839254
hg1939148
hg1839148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5052n100
Supporting Variantsnssv3619251, nssv3619250, nssv3619252
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)nsv1012666
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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