A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730077



Internal ID21400893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87924058..87938086hg38UCSC Ensembl
chr4:88845210..88859238hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3814029
hg1914029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256499, nssv16256171, nssv16255906, nssv16256777, nssv16257098, nssv16256267, nssv16258399, nssv16257516, nssv16256011, nssv16256997, nssv16258697, nssv16257558, nssv16256733, nssv16257548, nssv16257046, nssv16256362, nssv16257020, nssv16258608, nssv16256852, nssv16256665, nssv16258768, nssv16257761, nssv16257875, nssv16257055, nssv16257924, nssv16257482, nssv16257866, nssv16256100, nssv16257589, nssv16256656, nssv16258183, nssv16256045, nssv16256938, nssv16257304, nssv16255924, nssv16255884
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730077
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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