A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575441



Internal ID20948512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56926944..56927857hg38UCSC Ensembl
chr5:56222771..56223684hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269125
Samples
Known GenesMIER3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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