A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818831



Internal ID21264169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1638777..1638941hg38UCSC Ensembl
chrX:1757670..1757834hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699419
Samples
Known GenesASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818831
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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