A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595688



Internal ID16036411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150855565..150883705hg38UCSC Ensembl
Innerchr4:151776717..151804857hg19UCSC Ensembl
Innerchr4:151996167..152024307hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3828141
hg1928141
hg1828141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009402
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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