A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730157



Internal ID21400968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120023559..120188640hg38UCSC Ensembl
chrX:119157524..119322493hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38165082
hg19164970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257038, nssv16258628, nssv16257633, nssv16258678, nssv16256588, nssv16257964, nssv16258535, nssv16257859
SamplesNA19238, NA19240
Known GenesRHOXF1, RHOXF2, RHOXF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730157
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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