A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996271



Internal ID64963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42503844..42519029hg38UCSC Ensembl
chr7:42543443..42558628hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3815186
hg1915186
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996271
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001249


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