A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703432



Internal ID21225248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27210489..27210775hg38UCSC Ensembl
chrX:27228606..27228892hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819886
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703432
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.890625


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