A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562722



Internal ID21887077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9543504..9613292hg38UCSC Ensembl
chr7:9583134..9652922hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3869789
hg1969789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562722
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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