A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516855



Internal ID18815136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84828122..84886961hg38UCSC Ensembl
Innerchr10:86587878..86646717hg19UCSC Ensembl
Innerchr10:86577858..86636697hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3858840
hg1958840
hg1858840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047083
Supporting Variants
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)nssv3516855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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