A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525587



Internal ID22394965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178005724..178006241hg38UCSC Ensembl
chr4:178926878..178927395hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14318101, nssv14318098, nssv14318100, nssv14318097, nssv14318099
SamplesHG00512, NA19239, HG00731, HG00733, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525587
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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