A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593831



Internal ID21785874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42592846..42593454hg38UCSC Ensembl
chr8:42447989..42448597hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593831
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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