A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519587



Internal ID15446880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2097420..2145213hg38UCSC Ensembl
Innerchr6:2097654..2145447hg19UCSC Ensembl
Innerchr6:2042653..2090446hg18UCSC Ensembl
Innerchr6:2042653..2090446hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3847794
hg1947794
hg1847794
hg1747794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696937
Samples
Known GenesGMDS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519587
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