A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559796



Internal ID20932867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39013048..39013667hg38UCSC Ensembl
chr4:39014668..39015287hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5234n223
Supporting Variantsnssv18265123
Samples
Known GenesTMEM156
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559796
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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