A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701839



Internal ID15091805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6315089..6320329hg38UCSC Ensembl
Innerchr18:6315088..6320328hg19UCSC Ensembl
Innerchr18:6305088..6310328hg18UCSC Ensembl
Innerchr18:6305088..6310328hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385241
hg195241
hg185241
hg175241
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525681
Supporting Variants
Samples
Known GenesL3MBTL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701839
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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