A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524410



Internal ID15451703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196049369..196089324hg38UCSC Ensembl
Innerchr3:195776240..195816195hg19UCSC Ensembl
Innerchr3:197260637..197300592hg18UCSC Ensembl
Innerchr3:197264550..197304505hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3839956
hg1939956
hg1839956
hg1739956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700332
Samples
Known GenesTFRC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524410
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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