A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515606



Internal ID15443217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192881547..192891927hg38UCSC Ensembl
Innerchr3:192599336..192609716hg19UCSC Ensembl
Innerchr3:194082030..194092410hg18UCSC Ensembl
Innerchr3:194082038..194092418hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3810381
hg1910381
hg1810381
hg1710381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv308n21
Supporting Variantsnssv679731, nssv662540, nssv664065, nssv670250, nssv690019, nssv685879
Samples
Known GenesMB21D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515606
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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