A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055089



Internal ID19144308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9937318..9965411hg38UCSC Ensembl
Innerchr10:9979281..10007374hg19UCSC Ensembl
Innerchr10:10019287..10047380hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3828094
hg1928094
hg1828094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707687, nssv3707688
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055089
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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