A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219958



Internal ID22364811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10767840..10768010hg38UCSC Ensembl
chr10:10809803..10809973hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331079, nssv14331081, nssv14331080
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219958
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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