A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524830



Internal ID15452123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29396329..29400424hg38UCSC Ensembl
Innerchr18:26976294..26980389hg19UCSC Ensembl
Innerchr18:25230292..25234387hg18UCSC Ensembl
Innerchr18:25230292..25234387hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg384096
hg194096
hg184096
hg174096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700831
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524830
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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