A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050080



Internal ID19139299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65535206..65566414hg38UCSC Ensembl
Innerchr10:67294964..67326172hg19UCSC Ensembl
Innerchr10:66964970..66996178hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3831209
hg1931209
hg1831209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883n100
Supporting Variantsnssv3519365
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)nsv1050080
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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