A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820620



Internal ID21265958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84080388..84080388hg38UCSC Ensembl
chrX:83335396..83335396hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702727
Samples
Known GenesRPS6KA6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820620
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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