A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213924



Internal ID22360721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100550299..100550423hg38UCSC Ensembl
chr13:101202553..101202677hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14369722, nssv14369721
SamplesHG00512, HG00513
Known GenesGGACT
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213924
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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