A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518196



Internal ID15098803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:92252109..92261583hg38UCSC Ensembl
Innerchr1:92717666..92727140hg19UCSC Ensembl
Innerchr1:92490254..92499728hg18UCSC Ensembl
Innerchr1:92429687..92439161hg17UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg389475
hg199475
hg189475
hg179475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695620
Samples
Known GenesGLMN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518196
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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