A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526051



Internal ID15106658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27284255..27445496hg38UCSC Ensembl
Innerchr1:27610746..27772009hg19UCSC Ensembl
Innerchr1:27483333..27644596hg18UCSC Ensembl
Innerchr1:27294888..27456151hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38161242
hg19161264
hg18161264
hg17161264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702288
Samples
Known GenesCD164L2, FCN3, GPR3, LOC644961, MAP3K6, SYTL1, TMEM222, WASF2, WDTC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526051
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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