A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999377



Internal ID19158913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163869551..163922154hg38UCSC Ensembl
Innerchr3:163587339..163639942hg19UCSC Ensembl
Innerchr3:165070033..165122636hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3852604
hg1952604
hg1852604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614530
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)nsv999377
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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