A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560337



Internal ID20933408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105686156..105687702hg38UCSC Ensembl
chr4:106607313..106608859hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381547
hg191547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263443
Samples
Known GenesINTS12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560337
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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