A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008530



Internal ID21917873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138357541..138357601hg38UCSC Ensembl
chr5:137693230..137693290hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550383
Samples
Known GenesKDM3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008530
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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