A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595695



Internal ID16036418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150959613..150961797hg38UCSC Ensembl
Innerchr4:151880765..151882949hg19UCSC Ensembl
Innerchr4:152100215..152102399hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382185
hg192185
hg182185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9314n54
Supporting Variantsnssv1009409
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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