A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972201



Internal ID22747136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96495384..96543426hg38UCSC Ensembl
chr5:95831088..95879130hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3848043
hg1948043
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420353
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972201
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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