A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730244



Internal ID21401055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218792..6220368hg38UCSC Ensembl
chrX:6136833..6138409hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257803, nssv16258343, nssv16257840, nssv16257478, nssv16256534, nssv16256485, nssv16258401, nssv16256924, nssv16258782, nssv16257093, nssv16257284, nssv16256607, nssv16258544, nssv16256686, nssv16258536
SamplesHG00512, NA19239, HG00732, HG00733, HG00514
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730244
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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