A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704827



Internal ID15094793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132859348..133620799hg38UCSC Ensembl
Innerchr10:134672852..135434303hg19UCSC Ensembl
Innerchr10:134522842..135284293hg18UCSC Ensembl
Innerchr10:134522842..135323184hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38761452
hg19761452
hg18761452
hg17800343
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528260
Supporting Variants
Samples
Known GenesADAM8, CALY, CYP2E1, ECHS1, FUOM, GPR123, KNDC1, LOC399829, MIR202, MIR202HG, MIR3944, MTG1, PAOX, PRAP1, SCART1, SPRN, SPRNP1, SYCE1, TTC40, TUBGCP2, UTF1, VENTX, ZNF511
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704827
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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