A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417611



Internal ID22475481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137615671..137619439hg38UCSC Ensembl
chr4:138536825..138540593hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg383769
hg193769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417611
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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