A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035534



Internal ID19124753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27171221..27208761hg38UCSC Ensembl
Innerchr15:27416368..27453908hg19UCSC Ensembl
Innerchr15:24999114..25036654hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3837541
hg1937541
hg1837541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545634
Samples
Known GenesGABRG3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035534
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer