A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516551



Internal ID22574514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64294737..64326536hg38UCSC Ensembl
chrX:63514617..63546416hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3831800
hg1931800
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967634
Supporting Variants
Samples
Known GenesMTMR8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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