A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020518



Internal ID19109737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158074929..158592892hg38UCSC Ensembl
Innerchr7:157867621..158385584hg19UCSC Ensembl
Innerchr7:157560382..158078345hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38517964
hg19517964
hg18517964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674735, nssv3757740
Samples
Known GenesMIR5707, MIR595, PTPRN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020518
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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