A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495658



Internal ID22553591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143801316..143806592hg38UCSC Ensembl
chr5:143180881..143186157hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg385277
hg195277
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495658
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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