A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577214



Internal ID21769257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151278055..151278055hg38UCSC Ensembl
chr6:151599190..151599190hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6071491
Supporting Variants
Samples
Known GenesAKAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577214
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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