A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563513



Internal ID21887868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36854408..36854408hg38UCSC Ensembl
chr6:36822184..36822184hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563513
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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