A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976582



Internal ID22751517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35447988..35449219hg38UCSC Ensembl
chr6:35415765..35416996hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448215
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976582
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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