A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571525



Internal ID21763568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6537575..6537575hg38UCSC Ensembl
chr6:6537808..6537808hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068508
Supporting Variants
Samples
Known GenesLY86-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571525
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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