A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730085



Internal ID21400901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51995788..52215089hg38UCSC Ensembl
chrX:51738884..51958216hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38219302
hg19219333
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258883, nssv16258046, nssv16256141, nssv16258684, nssv16255909, nssv16258633, nssv16257242, nssv16257163, nssv16256277, nssv16256816, nssv16257074, nssv16257140, nssv16258152, nssv16256601, nssv16258084, nssv16256783, nssv16256773, nssv16256597, nssv16258348, nssv16256845, nssv16257066, nssv16257164, nssv16257257, nssv16258547, nssv16257601, nssv16258759, nssv16258881, nssv16258009
SamplesHG00512, NA19238, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesMAGED4, MAGED4B, SNORA11D, SNORA11E
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730085
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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