A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576813



Internal ID21768856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10630764..10636371hg38UCSC Ensembl
chr6:10630997..10636604hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576813
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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