A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521262



Internal ID15101869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91660960..91666634hg38UCSC Ensembl
Innerchr6:92370678..92376352hg19UCSC Ensembl
Innerchr6:92427399..92433073hg18UCSC Ensembl
Innerchr6:92427399..92433073hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385675
hg195675
hg185675
hg175675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693359, nssv689437
Samples
Known GenesCASC6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521262
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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