A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512292



Internal ID18463887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68410888..68752800hg38UCSC Ensembl
Innerchr10:70170645..70512557hg19UCSC Ensembl
Innerchr10:69840651..70182563hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38341913
hg19341913
hg18341913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049834
Supporting Variants
Samples
Known GenesCCAR1, DNA2, SLC25A16, TET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512292
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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