A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699519



Internal ID15089485
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
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)nssv699519
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer