A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516867



Internal ID15097474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194456593..194492803hg38UCSC Ensembl
Innerchr3:194177322..194213532hg19UCSC Ensembl
Innerchr3:195658611..195694821hg18UCSC Ensembl
Innerchr3:195658619..195694829hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3836211
hg1936211
hg1836211
hg1736211
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689131, nssv690646, nssv654543, nssv684870, nssv676613, nssv701031, nssv703033, nssv672710, nssv655187
Samples
Known GenesATP13A3, LINC00884
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516867
Frequency
Sample Size2026
Observed Gain1
Observed Loss8
Observed Complex0
Frequencyn/a


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