A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059695



Internal ID19148914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:25900132..25925254hg38UCSC Ensembl
Innerchr18:23480096..23505218hg19UCSC Ensembl
Innerchr18:21734094..21759216hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3825123
hg1925123
hg1825123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564137
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)nsv1059695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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