A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014408



Internal ID21923751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64848203..64855246hg38UCSC Ensembl
chr5:64144030..64151073hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg387044
hg197044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546066
Samples
Known GenesCWC27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014408
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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