A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695399



Internal ID15432051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196990442..197023970hg38UCSC Ensembl
Innerchr3:196717313..196750841hg19UCSC Ensembl
Innerchr3:198201710..198235238hg18UCSC Ensembl
Innerchr3:198205623..198239151hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3833529
hg1933529
hg1833529
hg1733529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517987
Supporting Variants
Samples
Known GenesMFI2, MFI2-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695399
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