A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565347



Internal ID20938418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38595366..38596147hg38UCSC Ensembl
chr4:38596987..38597768hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565347
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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