A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975682



Internal ID22750617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51881905..51886098hg38UCSC Ensembl
chr1:52347577..52351770hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384194
hg194194
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375743
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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