A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875487



Internal ID22650444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10912331..10913264hg38UCSC Ensembl
chrX:10930451..10931384hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434586
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875487
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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