A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881421



Internal ID22656396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46495904..46497412hg38UCSC Ensembl
chrX:46355339..46356847hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881421
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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