A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526013



Internal ID22395392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82908752..82908871hg38UCSC Ensembl
chr5:82204571..82204690hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7414n152
Supporting Variantsnssv14322710, nssv14322711, nssv14322712
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526013
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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