A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515671



Internal ID15443282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:126786329..126811417hg38UCSC Ensembl
Innerchr8:127798574..127823662hg19UCSC Ensembl
Innerchr8:127867756..127892844hg18UCSC Ensembl
Innerchr8:127867756..127892844hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3825089
hg1925089
hg1825089
hg1725089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664326, nssv661888
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515671
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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