A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028074



Internal ID19117292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24256258..24272598hg38UCSC Ensembl
Innerchr7:24295877..24312217hg19UCSC Ensembl
Innerchr7:24262402..24278742hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3816341
hg1916341
hg1816341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643282
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028074
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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