A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523383



Internal ID15450676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170244928..170276667hg38UCSC Ensembl
Innerchr6:170554016..170585755hg19UCSC Ensembl
Innerchr6:170395941..170427680hg18UCSC Ensembl
Innerchr6:170471648..170503387hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3831740
hg1931740
hg1831740
hg1731740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699132
Samples
Known GenesFLJ38122, LOC154449
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523383
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