A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561896



Internal ID334863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62993105..62993818hg38UCSC Ensembl
chr8:63905664..63906377hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561896
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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