A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974581



Internal ID22749516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72480203..72490776hg38UCSC Ensembl
chr5:71776030..71786603hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3810574
hg1910574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417634
Samples
Known GenesZNF366
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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