A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820182



Internal ID21265520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118647967..118647967hg38UCSC Ensembl
chrX:117781930..117781930hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706012
Samples
Known GenesDOCK11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820182
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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