A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697826



Internal ID15434478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6162007..6184093hg38UCSC Ensembl
Innerchr18:6162006..6184092hg19UCSC Ensembl
Innerchr18:6152006..6174092hg18UCSC Ensembl
Innerchr18:6152006..6174092hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3822087
hg1922087
hg1822087
hg1722087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521173
Supporting Variants
Samples
Known GenesL3MBTL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697826
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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