A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032866



Internal ID19122088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15297206..15582890hg38UCSC Ensembl
Innerchr7:15336831..15622515hg19UCSC Ensembl
Innerchr7:15303356..15589040hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38285685
hg19285685
hg18285685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6287n100
Supporting Variantsnssv3643179
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032866
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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