A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818926



Internal ID21264264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233764..47233816hg38UCSC Ensembl
chrX:47093163..47093215hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699624
Samples
Known GenesUSP11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818926
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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