A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517022



Internal ID15097629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149823865..150105136hg38UCSC Ensembl
Innerchr6:150145001..150426272hg19UCSC Ensembl
Innerchr6:150186694..150467965hg18UCSC Ensembl
Innerchr6:150237115..150518386hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38281272
hg19281272
hg18281272
hg17281272
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658419, nssv698324, nssv653630, nssv696319, nssv702769, nssv673246, nssv661372, nssv682937, nssv704657, nssv700224, nssv694489, nssv705168
Samples
Known GenesLRP11, RAET1E, RAET1E-AS1, RAET1G, RAET1K, RAET1L, ULBP1, ULBP2, ULBP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517022
Frequency
Sample Size2026
Observed Gain2
Observed Loss10
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer