A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516103



Internal ID15443396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133255801..133258115hg38UCSC Ensembl
Innerchr9:136131188..136133506hg19UCSC Ensembl
Innerchr9:135121009..135123327hg18UCSC Ensembl
Innerchr9:133160742..133163060hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg382315
hg192319
hg182319
hg172319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660810, nssv666231, nssv703923, nssv656531, nssv670428, nssv675786, nssv698808, nssv667456, nssv685831, nssv689077
Samples
Known GenesABO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516103
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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