A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730147



Internal ID21400958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89298590..91406286hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382107697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258210, nssv16256668, nssv16256617
SamplesHG00731, HG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730147
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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