A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819886



Internal ID21265224
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 StatusM
Merged Variants
Supporting Variantsnssv13703432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819886
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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