A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026130



Internal ID19115347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101327634..101498690hg38UCSC Ensembl
Innerchr7:100970915..101141971hg19UCSC Ensembl
Innerchr7:100757635..100928691hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38171057
hg19171057
hg18171057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3656097
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)nsv1026130
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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