A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500876



Internal ID22558813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106990769..107014744hg38UCSC Ensembl
chr6:107311969..107335948hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3823976
hg1923980
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844205
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500876
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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