A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730180



Internal ID21400991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179634372..179656672hg38UCSC Ensembl
chr5:179061373..179083673hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3822301
hg1922301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256526, nssv16256674, nssv16257444, nssv16258885, nssv16257186, nssv16258069, nssv16256894, nssv16257704, nssv16256539, nssv16258431, nssv16257669, nssv16257056, nssv16256630, nssv16257352, nssv16256885, nssv16257678, nssv16256690, nssv16258607
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesC5orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730180
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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