A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060485



Internal ID18803016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4297791..4360028hg38UCSC Ensembl
Innerchr18:4297791..4360028hg19UCSC Ensembl
Innerchr18:4287791..4350028hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3862238
hg1962238
hg1862238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725272
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060485
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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