A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005841



Internal ID71514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:153031262..153820289hg38UCSC Ensembl
chr7:152728347..153517374hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38789028
hg19789028
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005841
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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