A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820967



Internal ID21266306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97570727..97578529hg38UCSC Ensembl
chrX:96825726..96833528hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg387803
hg197803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709147
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820967
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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