A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510598



Internal ID18808879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105560231..105745168hg38UCSC Ensembl
Innerchr10:107319989..107504926hg19UCSC Ensembl
Innerchr10:107309979..107494916hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38184938
hg19184938
hg18184938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048131
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)nssv3510598
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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