A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996277



Internal ID64967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42540405..42540439hg38UCSC Ensembl
chr7:42580004..42580038hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.139401


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