A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574857



Internal ID20947928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37014987..37015649hg38UCSC Ensembl
chr5:37015089..37015751hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268846
Samples
Known GenesNIPBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574857
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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