A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557897



Internal ID20930968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108024006..108029795hg38UCSC Ensembl
chr4:108945162..108950951hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg385790
hg195790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263471
Samples
Known GenesHADH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557897
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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