A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020456



Internal ID19109675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101512775hg38UCSC Ensembl
Innerchr7:100968363..101156056hg19UCSC Ensembl
Innerchr7:100755083..100942776hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38187694
hg19187694
hg18187694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3656090
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020456
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer