A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523205



Internal ID15450498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10005019..10042251hg38UCSC Ensembl
Innerchr3:10046703..10083935hg19UCSC Ensembl
Innerchr3:10021703..10058935hg18UCSC Ensembl
Innerchr3:10021703..10058935hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837233
hg1937233
hg1837233
hg1737233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698925
Samples
Known GenesCIDECP, EMC3-AS1, FANCD2, LOC401052
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523205
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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