A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573871



Internal ID21765914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168458351..168458351hg38UCSC Ensembl
chr6:168859031..168859031hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061065
Supporting Variants
Samples
Known GenesSMOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573871
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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