A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870249



Internal ID22645185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101760328..101760568hg38UCSC Ensembl
chrX:101015301..101015541hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870249
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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