A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967634



Internal ID22742569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64294737..64326536hg38UCSC Ensembl
chrX:63514617..63546416hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3831800
hg1931800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516551
Samples
Known GenesMTMR8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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