A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1009407



Internal ID15956677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150958557..150961692hg38UCSC Ensembl
Innerchr4:151879709..151882844hg19UCSC Ensembl
Innerchr4:152099159..152102294hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383136
hg193136
hg183136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595693
Supporting Variants
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1009407
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