A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055086



Internal ID19144305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612155..6622533hg38UCSC Ensembl
Innerchr10:6654117..6664495hg19UCSC Ensembl
Innerchr10:6694123..6704501hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810379
hg1910379
hg1810379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv667n100
Supporting Variantsnssv3496247
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)nsv1055086
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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