A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818352



Internal ID21263690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107910814..107910814hg38UCSC Ensembl
chrX:107154044..107154044hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706537
Samples
Known GenesMID2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818352
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer