A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516282



Internal ID15443575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4227815..4229454hg38UCSC Ensembl
Innerchr6:4228049..4229688hg19UCSC Ensembl
Innerchr6:4173048..4174687hg18UCSC Ensembl
Innerchr6:4173048..4174687hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381640
hg191640
hg181640
hg171640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691084, nssv667327
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516282
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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