A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991714



Internal ID61903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136433..405503hg38UCSC Ensembl
chr7:136433..445469hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38269071
hg19309037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454390
Supporting Variants
Samples
Known GenesFAM20C, LOC100288524, LOC100507642, LOC442497
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991714
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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