A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525383



Internal ID15452676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6547011..6547132hg38UCSC Ensembl
Innerchr18:6547010..6547131hg19UCSC Ensembl
Innerchr18:6537010..6537131hg18UCSC Ensembl
Innerchr18:6537010..6537131hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38122
hg19122
hg18122
hg17122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701505
Samples
Known GenesC18orf64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525383
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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