A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573145



Internal ID20946216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17598777..17599272hg38UCSC Ensembl
chr4:17600400..17600895hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264508
Samples
Known GenesLAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573145
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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