A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561480



Internal ID20934551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21916052..21918191hg38UCSC Ensembl
chr4:21917675..21919814hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265571
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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