A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525889



Internal ID15106496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:63845132..63948110hg38UCSC Ensembl
Innerchr18:61512366..61615344hg19UCSC Ensembl
Innerchr18:59663346..59766324hg18UCSC Ensembl
Innerchr18:59663346..59766324hg17UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38102979
hg19102979
hg18102979
hg17102979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702092
Samples
Known GenesSERPINB10, SERPINB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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