A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149602



Internal ID15506611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74016599..74055382hg38UCSC Ensembl
Innerchr15:74308940..74347723hg19UCSC Ensembl
Innerchr15:72095993..72134776hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3838784
hg1938784
hg1838784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569971
Supporting Variants
Samples1780854065_A
Known GenesPML
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149602
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