A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575336



Internal ID21767379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109467740..109469232hg38UCSC Ensembl
chr6:109788943..109790435hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381493
hg191493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016610
Supporting Variants
Samples
Known GenesZBTB24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575336
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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