A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398066



Internal ID22455936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:81291418..81370189hg38UCSC Ensembl
chr2:81518542..81597313hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3878772
hg1978772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398066
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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