A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730167



Internal ID21400978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145693712..145694599hg38UCSC Ensembl
chr4:146614864..146615751hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38888
hg19888
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257674, nssv16258071, nssv16256097, nssv16257451, nssv16258179, nssv16257931
SamplesNA19238, NA19239, NA19240, HG00733, HG00514
Known GenesC4orf51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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