A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563466



Internal ID20936537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147504873..147505668hg38UCSC Ensembl
chr4:148426025..148426820hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264803
Samples
Known GenesEDNRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563466
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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