A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566926



Internal ID21758969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63785718..63785890hg38UCSC Ensembl
chr6:64495611..64495783hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016574
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566926
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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