A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574908



Internal ID20947979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132365204..132365671hg38UCSC Ensembl
chr5:131700896..131701363hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267949
Samples
Known GenesLOC553103, MIR3936
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574908
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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