A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524394



Internal ID15105001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36323945..36382165hg38UCSC Ensembl
Innerchr1:36789546..36847766hg19UCSC Ensembl
Innerchr1:36562133..36620353hg18UCSC Ensembl
Innerchr1:36458639..36516859hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3858221
hg1958221
hg1858221
hg1758221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700312
Samples
Known GenesEVA1B, STK40
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524394
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