A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982126



Internal ID55444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37182175..37496244hg38UCSC Ensembl
chr6:37149951..37464020hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38314070
hg19314070
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563741
Supporting Variants
Samples
Known GenesCCDC167, CMTR1, RNF8, TBC1D22B, TMEM217
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982126
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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