A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042755



Internal ID21952067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35690776..35690827hg38UCSC Ensembl
chr19:36181678..36181729hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042755
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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