A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018360



Internal ID19107577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76819246..77118682hg38UCSC Ensembl
Innerchr7:76448563..76747999hg19UCSC Ensembl
Innerchr7:76286499..76585935hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38299437
hg19299437
hg18299437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6501n100
Supporting Variantsnssv3657087
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018360
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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