A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567061



Internal ID21759104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266347..16266401hg38UCSC Ensembl
chr6:16266578..16266632hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017888
Supporting Variants
Samples
Known GenesGMPR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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