A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562888



Internal ID21887243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63390610..63390674hg38UCSC Ensembl
chr6:64100515..64100579hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013888
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562888
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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