A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517276



Internal ID15097883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:41931609..41949233hg38UCSC Ensembl
Innerchr4:41933626..41951250hg19UCSC Ensembl
Innerchr4:41628383..41646007hg18UCSC Ensembl
Innerchr4:41774554..41792178hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3817625
hg1917625
hg1817625
hg1717625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv655868, nssv659904, nssv654187
Samples
Known GenesTMEM33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517276
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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