A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524912



Internal ID15452205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57658436..57661366hg38UCSC Ensembl
Innerchr15:57950634..57953564hg19UCSC Ensembl
Innerchr15:55737926..55740856hg18UCSC Ensembl
Innerchr15:55737926..55740856hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382931
hg192931
hg182931
hg172931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv150n21
Supporting Variantsnssv700924
Samples
Known GenesGCOM1, MYZAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524912
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