A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515488



Internal ID15443335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37010969..37021811hg38UCSC Ensembl
Innerchr6:36978745..36989587hg19UCSC Ensembl
Innerchr6:37086723..37097565hg18UCSC Ensembl
Innerchr6:37086723..37097565hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3810843
hg1910843
hg1810843
hg1710843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688668, nssv680098, nssv678307, nssv657792, nssv690764, nssv674575, nssv665909, nssv653290
Samples
Known GenesFGD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515488
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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