A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694426



Internal ID15084392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3526777..5922015hg38UCSC Ensembl
Innerchr18:3526775..5922014hg19UCSC Ensembl
Innerchr18:3516775..5912014hg18UCSC Ensembl
Innerchr18:3516775..5912014hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382395239
hg192395240
hg182395240
hg172395240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521255
Supporting Variants
Samples
Known GenesC18orf42, DLGAP1, DLGAP1-AS1, DLGAP1-AS3, DLGAP1-AS4, DLGAP1-AS5, EPB41L3, LINC00526, LINC00667, LOC645355, MIR3976, MIR6718, TMEM200C, ZBTB14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694426
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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