A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016921



Internal ID19106138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13054314..13091020hg38UCSC Ensembl
Innerchr7:13093939..13130645hg19UCSC Ensembl
Innerchr7:13060464..13097170hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3836707
hg1936707
hg1836707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6277n100
Supporting Variantsnssv3643031
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)nsv1016921
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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