A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572748



Internal ID20945819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153370265..153370654hg38UCSC Ensembl
chr4:154291417..154291806hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263890
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572748
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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