A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702518



Internal ID15092484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49446036..49457538hg38UCSC Ensembl
Innerchr15:49738233..49749735hg19UCSC Ensembl
Innerchr15:47525525..47537027hg18UCSC Ensembl
Innerchr15:47525525..47537027hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811503
hg1911503
hg1811503
hg1711503
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526246
Supporting Variants
Samples
Known GenesFAM227B, FGF7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702518
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