A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556682



Internal ID21881037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15755736..15756180hg38UCSC Ensembl
chr4:15757359..15757803hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5995683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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