A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018254



Internal ID19107471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110512818..110555309hg38UCSC Ensembl
Innerchr7:110152875..110195366hg19UCSC Ensembl
Innerchr7:109940111..109982602hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3842492
hg1942492
hg1842492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6563n100
Supporting Variantsnssv3645212
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)nsv1018254
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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