A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730276



Internal ID21401087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52488524..52538369hg38UCSC Ensembl
chrX:52231667..52567379hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3849846
hg19335713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257775, nssv16257928, nssv16257720, nssv16258573, nssv16257142, nssv16256985, nssv16258221, nssv16256517, nssv16257297, nssv16258613, nssv16257060, nssv16256154, nssv16256964, nssv16256771, nssv16257372, nssv16257125, nssv16258615, nssv16258053, nssv16258880, nssv16257330, nssv16257273, nssv16255983, nssv16258820, nssv16257311, nssv16256625, nssv16256428, nssv16258594, nssv16256384
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00513, HG00514
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730276
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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