A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521856



Internal ID15449149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:38027232..38033971hg38UCSC Ensembl
Innerchr1:38492904..38499643hg19UCSC Ensembl
Innerchr1:38265491..38272230hg18UCSC Ensembl
Innerchr1:38161997..38168736hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386740
hg196740
hg186740
hg176740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694630
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521856
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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