A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021634



Internal ID18764168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15554099..15576162hg38UCSC Ensembl
Innerchr8:15411608..15433671hg19UCSC Ensembl
Innerchr8:15455979..15478042hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3822064
hg1922064
hg1822064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7107n100
Supporting Variantsnssv3675900
Samples
Known GenesTUSC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021634
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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