A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730209



Internal ID21401020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55457117..55521060hg38UCSC Ensembl
chrX:55483550..55547493hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3863944
hg1963944
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257054, nssv16257991, nssv16256909, nssv16255897, nssv16257384, nssv16258632, nssv16258063, nssv16257776, nssv16256451, nssv16257593, nssv16257215, nssv16256652, nssv16256163, nssv16257063, nssv16257195, nssv16257519, nssv16258796, nssv16258440, nssv16256379, nssv16258233, nssv16256274, nssv16258727, nssv16256072, nssv16256344
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00514
Known GenesUSP51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730209
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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