A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485386



Internal ID22543297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37140629..37153443hg38UCSC Ensembl
chr20:35769032..35781846hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812815
hg1912815
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887210
Supporting Variants
Samples
Known GenesMROH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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