A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730207



Internal ID21401018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154555766..154645807hg38UCSC Ensembl
chrX:153783981..153874081hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3890042
hg1990101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257888, nssv16258048, nssv16257322, nssv16256986, nssv16258756, nssv16257291, nssv16256209, nssv16256900, nssv16258427, nssv16258418, nssv16256082, nssv16257011, nssv16256459, nssv16258806, nssv16256098, nssv16256124, nssv16258387, nssv16257891, nssv16255903, nssv16258388
SamplesHG00512, NA19238, NA19239, NA19240, HG00514
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730207
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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