A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998526



Internal ID66562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57622242..58024242hg38UCSC Ensembl
chr7:57681948..58054331hg19UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38402001
hg19372384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998526
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000469


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