A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730106



Internal ID21400859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72972887..73080247hg38UCSC Ensembl
chrX:72192722..72300086hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38107361
hg19107365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258617, nssv16256230, nssv16255985, nssv16257376, nssv16256983, nssv16258742, nssv16256156, nssv16256865, nssv16257321, nssv16258153, nssv16256204, nssv16256562, nssv16255919, nssv16255969, nssv16256795, nssv16258235
SamplesNA19238, HG00731, NA19240, HG00733
Known GenesPABPC1L2A, PABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730106
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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