A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574765



Internal ID20947836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37950086..37952792hg38UCSC Ensembl
chr4:37951707..37954413hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382707
hg192707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265097
Samples
Known GenesTBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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