A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040785



Internal ID18783316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77596297..77851680hg38UCSC Ensembl
Innerchr10:79356055..79611438hg19UCSC Ensembl
Innerchr10:79026061..79281444hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38255384
hg19255384
hg18255384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv929n100
Supporting Variantsnssv3506173
Samples
Known GenesDLG5, KCNMA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040785
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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