A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380219



Internal ID22438089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35697173..35700463hg38UCSC Ensembl
chr1:36162774..36166064hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383291
hg193291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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