A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041282



Internal ID19130501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54144489..54183938hg38UCSC Ensembl
Innerchr15:54436686..54476135hg19UCSC Ensembl
Innerchr15:52223978..52263427hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3839450
hg1939450
hg1839450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552432
Samples
Known GenesUNC13C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041282
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