A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026450



Internal ID19115668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101322320..101494033hg38UCSC Ensembl
Innerchr7:100965601..101137314hg19UCSC Ensembl
Innerchr7:100752321..100924034hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38171714
hg19171714
hg18171714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3755457, nssv3655311
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)nsv1026450
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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