A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700260



Internal ID15090226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..14978848hg38UCSC Ensembl
Innerchr10:14990369..15020847hg19UCSC Ensembl
Innerchr10:15030375..15060853hg18UCSC Ensembl
Innerchr10:15030375..15060853hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3830479
hg1930479
hg1830479
hg1730479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520429
Supporting Variants
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700260
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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