A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730051



Internal ID21400867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63159232..63249804hg38UCSC Ensembl
chrX:62378699..62469681hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3890573
hg1990983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257442, nssv16257113, nssv16258200, nssv16257064, nssv16258333, nssv16256291, nssv16258738, nssv16258369, nssv16258246, nssv16257849, nssv16258685, nssv16258597, nssv16257591, nssv16257254, nssv16256645, nssv16257967
SamplesNA19238, NA19239, NA19240, HG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730051
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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