A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020824



Internal ID19110042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76130758..76173514hg38UCSC Ensembl
Innerchr7:75760076..75802832hg19UCSC Ensembl
Innerchr7:75598012..75640768hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3842757
hg1942757
hg1842757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6469n100
Supporting Variantsnssv3656494
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)nsv1020824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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