A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026259



Internal ID19115476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19161287..19185179hg38UCSC Ensembl
Innerchr7:19200910..19224802hg19UCSC Ensembl
Innerchr7:19167435..19191327hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3823893
hg1923893
hg1823893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6300n100
Supporting Variantsnssv3643244
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)nsv1026259
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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