A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520429



Internal ID15101036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..15018884hg38UCSC Ensembl
Innerchr10:14990369..15060883hg19UCSC Ensembl
Innerchr10:15030375..15100889hg18UCSC Ensembl
Innerchr10:15030375..15100889hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3870515
hg1970515
hg1870515
hg1770515
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705897, nssv700260, nssv699519, nssv677144, nssv671367
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520429
Frequency
Sample Size2026
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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