A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876434



Internal ID22651395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38393287..38394693hg38UCSC Ensembl
chrX:38252540..38253946hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381407
hg191407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457677
Samples
Known GenesOTC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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