A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562769



Internal ID20935840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148745860..149225391hg38UCSC Ensembl
chr4:149667012..150146543hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38479532
hg19479532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5512n223
Supporting Variantsnssv18263755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562769
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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