A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524894



Internal ID15105501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95875148..95877962hg38UCSC Ensembl
Innerchr9:98637430..98640244hg19UCSC Ensembl
Innerchr9:97677251..97680065hg18UCSC Ensembl
Innerchr9:95716985..95719799hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg382815
hg192815
hg182815
hg172815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700900
Samples
Known GenesERCC6L2, LINC00476
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524894
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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