A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019184



Internal ID19108402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8641604..8725910hg38UCSC Ensembl
Innerchr7:8681234..8765540hg19UCSC Ensembl
Innerchr7:8647759..8732065hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3884307
hg1984307
hg1884307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642748
Samples
Known GenesNXPH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019184
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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