A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522833



Internal ID15450126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:135661977..135680889hg38UCSC Ensembl
Innerchr6:135983115..136002027hg19UCSC Ensembl
Innerchr6:136024808..136043720hg18UCSC Ensembl
Innerchr6:136024808..136043720hg17UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3818913
hg1918913
hg1818913
hg1718913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698483
Samples
Known GenesLINC00271, MIR548H4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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