A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018458



Internal ID19107675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159109202..159327018hg38UCSC Ensembl
Innerchr7:158901893..159119708hg19UCSC Ensembl
Innerchr7:158594654..158812469hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38217817
hg19217816
hg18217816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674790
Samples
Known GenesVIPR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018458
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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