A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062043



Internal ID19151262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1905345..1994942hg38UCSC Ensembl
Innerchr18:1905346..1994943hg19UCSC Ensembl
Innerchr18:1895346..1984943hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3889598
hg1989598
hg1889598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3564020
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)nsv1062043
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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