A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152604



Internal ID15880290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34125316..34270180hg38UCSC Ensembl
Innerchr4:34126938..34271802hg19UCSC Ensembl
Innerchr4:33803333..33948197hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38144865
hg19144865
hg18144865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593907
Supporting Variants
SamplesNINDS_189
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152604
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