A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035778



Internal ID19124997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65536569..65567409hg38UCSC Ensembl
Innerchr10:67296327..67327167hg19UCSC Ensembl
Innerchr10:66966333..66997173hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3830841
hg1930841
hg1830841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883n100
Supporting Variantsnssv3504131
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)nsv1035778
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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