A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525552



Internal ID22394930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154583464..154583536hg38UCSC Ensembl
chr5:153963024..153963096hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7576n152
Supporting Variantsnssv14324450, nssv14324449, nssv14324448
SamplesHG00512, NA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525552
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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