A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439171



Internal ID22497041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70539389..70540255hg38UCSC Ensembl
chr8:71451624..71452490hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439171
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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