A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876904



Internal ID22651866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154751228..154756719hg38UCSC Ensembl
chrX:153979503..153984994hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385492
hg195492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436299
Samples
Known GenesGAB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876904
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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