A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968528



Internal ID22743463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97795319..97795938hg38UCSC Ensembl
chr6:98243195..98243814hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444367
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968528
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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