A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563741



Internal ID336671
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 StatusM
Merged Variants
Supporting Variantsnssv16982126
Samples
Known GenesCCDC167, CMTR1, RNF8, TBC1D22B, TMEM217
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563741
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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