A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595524



Internal ID16382933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137150461..137179418hg38UCSC Ensembl
Innerchr4:138071615..138100572hg19UCSC Ensembl
Innerchr4:138291065..138320022hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3828958
hg1928958
hg1828958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9280n54
Supporting Variantsnssv1007638
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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