A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497331



Internal ID22555265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:50530040..50540729hg38UCSC Ensembl
chr5:49825874..49836563hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3810690
hg1910690
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497331
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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