A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519226



Internal ID15099833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108739559..108766158hg38UCSC Ensembl
Innerchr4:109660715..109687314hg19UCSC Ensembl
Innerchr4:109880164..109906763hg18UCSC Ensembl
Innerchr4:110018319..110044918hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3826600
hg1926600
hg1826600
hg1726600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696716
Samples
Known GenesETNPPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519226
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