A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026003



Internal ID18768535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95733543..96100442hg38UCSC Ensembl
Innerchr7:95362855..95729754hg19UCSC Ensembl
Innerchr7:95200791..95567690hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38366900
hg19366900
hg18366900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655252
Samples
Known GenesDYNC1I1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026003
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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