A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004070



Internal ID21913413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161711736..161715642hg38UCSC Ensembl
chr5:161138742..161142648hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg383907
hg193907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004070
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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