A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030664



Internal ID21940007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44833671..44853086hg38UCSC Ensembl
chr13:45407807..45427222hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3819416
hg1919416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608945
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030664
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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