A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060990



Internal ID19150209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68280434..68511817hg38UCSC Ensembl
Innerchr18:65947671..66179054hg19UCSC Ensembl
Innerchr18:64098651..64330034hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38231384
hg19231384
hg18231384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3392n100
Supporting Variantsnssv3562787, nssv3562786
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)nsv1060990
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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