A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486708



Internal ID22544623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56525687..56536614hg38UCSC Ensembl
chr20:55100743..55111670hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3810928
hg1910928
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881683
Supporting Variants
Samples
Known GenesFAM209A, FAM209B, GCNT7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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