A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017544



Internal ID19106761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101322320..101473041hg38UCSC Ensembl
Innerchr7:100965601..101116322hg19UCSC Ensembl
Innerchr7:100752321..100903042hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38150722
hg19150722
hg18150722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3755452
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)nsv1017544
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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