A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518413



Internal ID15445706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152515952..152525209hg38UCSC Ensembl
Innerchr1:152488428..152497685hg19UCSC Ensembl
Innerchr1:150755052..150764309hg18UCSC Ensembl
Innerchr1:149301501..149310758hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389258
hg199258
hg189258
hg179258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695848
Samples
Known GenesCRCT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518413
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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