A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584097



Internal ID21776140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62901641..62901641hg38UCSC Ensembl
chr8:63814200..63814200hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060880
Supporting Variants
Samples
Known GenesNKAIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584097
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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