A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029105



Internal ID19118324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13054314..13083783hg38UCSC Ensembl
Innerchr7:13093939..13123408hg19UCSC Ensembl
Innerchr7:13060464..13089933hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3829470
hg1929470
hg1829470
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6277n100
Supporting Variantsnssv3643001, nssv3642998, nssv3642996, nssv3642995, nssv3642999, nssv3643000, nssv3642993, nssv3642997, nssv3642994
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)nsv1029105
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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