A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371731



Internal ID22597400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:64951517..64956250hg38UCSC Ensembl
chr13:65525649..65530382hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945574
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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