A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820596



Internal ID21265934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74796125..74796125hg38UCSC Ensembl
chrX:74015960..74015960hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704059
Samples
Known GenesKIAA2022
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820596
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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