A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730272



Internal ID21401083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76141674..76153292hg38UCSC Ensembl
chrX:75361509..75373127hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3811619
hg1911619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257453, nssv16256236, nssv16257510, nssv16257162, nssv16258406, nssv16258000, nssv16256201, nssv16256972, nssv16258252, nssv16256404, nssv16258445, nssv16258516, nssv16257993, nssv16256165
SamplesNA19238, HG00731, HG00732, HG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730272
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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