A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528169



Internal ID15108776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:551688..2240220hg38UCSC Ensembl
Innerchr18:551688..2240220hg19UCSC Ensembl
Innerchr18:541688..2230220hg18UCSC Ensembl
Innerchr18:541688..2230220hg17UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381688533
hg191688533
hg181688533
hg171688533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704718
Samples
Known GenesADCYAP1, C18orf56, CETN1, CLUL1, ENOSF1, LINC00470, TYMS, YES1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528169
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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