A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018040



Internal ID18760573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38258222..38312406hg38UCSC Ensembl
Innerchr7:38297823..38352007hg19UCSC Ensembl
Innerchr7:38264348..38318532hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3854185
hg1954185
hg1854185
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6328n100
Supporting Variantsnssv3643455, nssv3643456
Samples
Known GenesTARP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018040
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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