A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526020



Internal ID15453313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:135758626..135760481hg38UCSC Ensembl
Innerchr8:136770869..136772724hg19UCSC Ensembl
Innerchr8:136840051..136841906hg18UCSC Ensembl
Innerchr8:136840051..136841906hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg381856
hg191856
hg181856
hg171856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702250
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526020
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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