A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880536



Internal ID22655506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42473378..42475077hg38UCSC Ensembl
chrX:42332630..42334329hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880536
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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