A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17499849



Internal ID22557785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56020134..56029126hg38UCSC Ensembl
chr5:55315962..55324953hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg388993
hg198992
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17499849
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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