A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210512



Internal ID22358384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37563751..37563819hg38UCSC Ensembl
chr19:38054653..38054721hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286485
SamplesHG00513
Known GenesZNF540, ZNF571-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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