A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573288



Internal ID21765331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1096018..1096018hg38UCSC Ensembl
chr6:1096253..1096253hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068530
Supporting Variants
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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