A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999329



Internal ID67124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88430540..88430546hg38UCSC Ensembl
chr7:88059855..88059861hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg387
hg197
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999329
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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