A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17571793



Internal ID21763836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2825484..2830453hg38UCSC Ensembl
chr6:2825718..2830687hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384970
hg194970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17571793
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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