A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877435



Internal ID22652400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155074204..155075315hg38UCSC Ensembl
chrX:154302479..154303590hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381112
hg191112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445719
Samples
Known GenesBRCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877435
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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