A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970638



Internal ID47754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95797940..95797942hg38UCSC Ensembl
chr5:95133644..95133646hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383
hg193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970638
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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