A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494865



Internal ID22552797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130597296..130610798hg38UCSC Ensembl
chr5:129932989..129946491hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3813503
hg1913503
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494865
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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