A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558444



Internal ID21882799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137972608..137972677hg38UCSC Ensembl
chr6:138293745..138293814hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001907
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558444
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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