A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516556



Internal ID15443849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:75360739..75369876hg38UCSC Ensembl
Innerchr11:75071783..75080920hg19UCSC Ensembl
Innerchr11:74749431..74758568hg18UCSC Ensembl
Innerchr11:74749431..74758568hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg389138
hg199138
hg189138
hg179138
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669132, nssv702360, nssv698102, nssv674926
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516556
Frequency
Sample Size2026
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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