A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757218



Internal ID20533078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120087101..120149200hg38UCSC Ensembl
chrX:119221059..119283106hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3862100
hg1962048
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293590
Samples
Known GenesRHOXF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757218
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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