A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527649



Internal ID15454942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15245489..15319252hg38UCSC Ensembl
Innerchr18:15245488..15319251hg19UCSC Ensembl
Innerchr18:15235488..15309251hg18UCSC Ensembl
Innerchr18:15235488..15309251hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3873764
hg1973764
hg1873764
hg1773764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704120
Samples
Known GenesLOC644669
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527649
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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