A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968109



Internal ID22743044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2635574..2637635hg38UCSC Ensembl
chr1:2567013..2569074hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382062
hg192062
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360188
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968109
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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