A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655337



Internal ID18953618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101492117hg38UCSC Ensembl
Innerchr7:100968363..101135398hg19UCSC Ensembl
Innerchr7:100755083..100922118hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38167036
hg19167036
hg18167036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032481
Supporting Variants
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)nssv3655337
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