A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984150



Internal ID56807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73420967..73426605hg38UCSC Ensembl
chr6:74130690..74136328hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385639
hg195639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466345
Supporting Variants
Samples
Known GenesMB21D1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984150
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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