A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492309



Internal ID22550236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102927846..102931659hg38UCSC Ensembl
chr5:102263550..102267363hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg383814
hg193814
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840843
Supporting Variants
Samples
Known GenesPAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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