A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv842503



Internal ID16136459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49242505..49253908hg38UCSC Ensembl
Innerchr15:49534702..49546105hg19UCSC Ensembl
Innerchr15:47321994..47333397hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811404
hg1911404
hg1811404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569344
Supporting Variants
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv842503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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