A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730113



Internal ID21400924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101597522..101616276hg38UCSC Ensembl
chrX:100852500..100871266hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3818755
hg1918767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257853, nssv16258394, nssv16256500, nssv16256437, nssv16258479, nssv16258751, nssv16256519, nssv16257855, nssv16257765, nssv16257390, nssv16256402, nssv16255865, nssv16257933, nssv16258790, nssv16257298, nssv16258175, nssv16256146, nssv16256445, nssv16257810, nssv16257948, nssv16258668, nssv16256505, nssv16256629, nssv16258056, nssv16258587, nssv16258305, nssv16258276, nssv16257169, nssv16255945, nssv16257091, nssv16257378, nssv16256643
SamplesHG00512, NA19238, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesARMCX6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730113
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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