A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv845292



Internal ID15792562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75940264..76258597hg38UCSC Ensembl
Innerchr15:76232605..76550938hg19UCSC Ensembl
Innerchr15:74019660..74337993hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38318334
hg19318334
hg18318334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569998
Supporting Variants
Samples
Known GenesC15orf27, ETFA, NRG4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv845292
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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