A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487304



Internal ID22545220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61948405..61960745hg38UCSC Ensembl
chr20:60523461..60535801hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3812341
hg1912341
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877089
Supporting Variants
Samples
Known GenesMIR1257
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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