A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730235



Internal ID21401046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102230490..102405716hg38UCSC Ensembl
chrX:101485484..101660637hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38175227
hg19175154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256180, nssv16257914, nssv16256131, nssv16256923, nssv16257599, nssv16258484, nssv16258121, nssv16257260, nssv16256935, nssv16256057, nssv16256693, nssv16257241, nssv16257317, nssv16256198, nssv16257248, nssv16256951, nssv16257876, nssv16257147
SamplesHG00512, NA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesNXF2, NXF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730235
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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