A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556254



Internal ID20929325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151316933..151317806hg38UCSC Ensembl
chr5:150696494..150697367hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268712
Samples
Known GenesSLC36A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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