A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380778



Internal ID22438648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64389012..64404147hg38UCSC Ensembl
chr1:64854695..64869830hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815136
hg1915136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380778
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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