A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730087



Internal ID21400903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152702624..152780919hg38UCSC Ensembl
chrX:151871102..151949442hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3878296
hg1978341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257461, nssv16256363, nssv16256840, nssv16258569, nssv16257683, nssv16257779, nssv16256932, nssv16258253, nssv16256247, nssv16257897, nssv16258362, nssv16257500, nssv16256592, nssv16258457, nssv16257816, nssv16256725, nssv16258588, nssv16256222, nssv16258432, nssv16256062, nssv16258855, nssv16258683
SamplesHG00512, NA19238, HG00732, HG00733, HG00513, HG00514
Known GenesCSAG1, CSAG2, CSAG3, CSAG4, MAGEA12, MAGEA2, MAGEA2B, MAGEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730087
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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