A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485340



Internal ID22543251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35672301..35683557hg38UCSC Ensembl
chr20:34260223..34271479hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3811257
hg1911257
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872989
Supporting Variants
Samples
Known GenesNFS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485340
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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