A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560762



Internal ID21885117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106718434..106718434hg38UCSC Ensembl
chr6:107166309..107166309hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381926
hg191926
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075004
Supporting Variants
Samples
Known GenesLOC100422737
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560762
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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