A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882952



Internal ID22657929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94145915..94149721hg38UCSC Ensembl
chrX:93400914..93404720hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882952
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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