A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066057



Internal ID19155276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1905345..1980374hg38UCSC Ensembl
Innerchr18:1905346..1980375hg19UCSC Ensembl
Innerchr18:1895346..1970375hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3875030
hg1975030
hg1875030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3563964, nssv3725207, nssv3725209, nssv3725206, nssv3725208
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)nsv1066057
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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