A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557986



Internal ID20931057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136474437..136474861hg38UCSC Ensembl
chr5:135810126..135810550hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557986
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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