A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709147



Internal ID21230925
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 StatusS
Merged Variantsnsv2820967
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709147
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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