A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061850



Internal ID19151069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76496780..76533640hg38UCSC Ensembl
Innerchr18:74208737..74245597hg19UCSC Ensembl
Innerchr18:72337725..72374585hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3836861
hg1936861
hg1836861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563031
Samples
Known GenesFLJ44313, LINC00908
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061850
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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