A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557014



Internal ID20930085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54510591..54647487hg38UCSC Ensembl
chr5:53806421..53943316hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38136897
hg19136896
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269074
Samples
Known GenesSNX18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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