A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560607



Internal ID20933678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1844757..1845882hg38UCSC Ensembl
chr4:1846484..1847609hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265507
Samples
Known GenesLETM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560607
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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