A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977901



Internal ID22752837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100950761..100952610hg38UCSC Ensembl
chr8:101962989..101964838hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381850
hg191850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435172
Samples
Known GenesYWHAZ
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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