A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020879



Internal ID19110097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126404094..126423377hg38UCSC Ensembl
Innerchr7:126044148..126063431hg19UCSC Ensembl
Innerchr7:125831384..125850667hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3819284
hg1919284
hg1819284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6614n100
Supporting Variantsnssv3662173
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)nsv1020879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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