A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416241



Internal ID22474111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:185635..185635hg38UCSC Ensembl
chr6:185635..185635hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416241
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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