A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575990



Internal ID21768033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90377810..90377810hg38UCSC Ensembl
chr6:91087529..91087529hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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