A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706217



Internal ID19004498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105385380..105548353hg38UCSC Ensembl
Innerchr10:107145138..107308111hg19UCSC Ensembl
Innerchr10:107135128..107298101hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38162974
hg19162974
hg18162974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048698
Supporting Variants
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)nssv3706217
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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