A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868553



Internal ID22643489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:8801199..8801269hg38UCSC Ensembl
chrX:8769240..8769310hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464139
Samples
Known GenesFAM9A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868553
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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