A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985598



Internal ID57808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75066132..75073428hg38UCSC Ensembl
chr6:75775848..75783144hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg387297
hg197297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985598
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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