A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053675



Internal ID18796206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18414966..18433983hg38UCSC Ensembl
Innerchr10:18703895..18722912hg19UCSC Ensembl
Innerchr10:18743901..18762918hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3819018
hg1919018
hg1819018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520134
Samples
Known GenesCACNB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053675
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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