A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091895



Internal ID15945081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101484174hg38UCSC Ensembl
Innerchr7:100968363..101127455hg19UCSC Ensembl
Innerchr7:100755083..100914175hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38159093
hg19159093
hg18159093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607980
Supporting Variants
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091895
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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