A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527295



Internal ID15454588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15002863..15002966hg38UCSC Ensembl
Innerchr19:15113675..15113778hg19UCSC Ensembl
Innerchr19:14974675..14974778hg18UCSC Ensembl
Innerchr19:14974675..14974778hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
hg17104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703710
Samples
Known GenesSLC1A6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527295
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