A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545542



Internal ID21869897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74301589..74301691hg38UCSC Ensembl
chr5:73597414..73597516hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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