A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045668



Internal ID18788199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:119611032..119859464hg38UCSC Ensembl
Innerchr10:121370544..121618976hg19UCSC Ensembl
Innerchr10:121360534..121608966hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38248433
hg19248433
hg18248433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515434
Samples
Known GenesBAG3, INPP5F, MCMBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045668
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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