A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516507



Internal ID18814788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89183210..89197932hg38UCSC Ensembl
Innerchr10:90942967..90957689hg19UCSC Ensembl
Innerchr10:90932947..90947669hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3814723
hg1914723
hg1814723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049521
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)nssv3516507
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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