A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595508



Internal ID16382917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134854083..135157838hg38UCSC Ensembl
Innerchr4:135775238..136078993hg19UCSC Ensembl
Innerchr4:135994688..136298443hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38303756
hg19303756
hg18303756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153509
SamplesNINDS_147
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595508
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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