A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730160



Internal ID21400971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233251..40236154hg38UCSC Ensembl
chr4:40234871..40237774hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382904
hg192904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16255845, nssv16257961, nssv16257894, nssv16258472, nssv16258549, nssv16256724, nssv16257181, nssv16258805, nssv16255864, nssv16256178, nssv16257629, nssv16256899, nssv16256554, nssv16258017, nssv16256826, nssv16258421
SamplesNA19238, NA19239, HG00731, NA19240, HG00733
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730160
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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