A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207670



Internal ID22356027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32537444..32543395hg38UCSC Ensembl
chr5:32537550..32543501hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg385952
hg195952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14321252, nssv14321253
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207670
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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