A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874717



Internal ID22649670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46600800..46600870hg38UCSC Ensembl
chrX:46460235..46460305hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450294
Samples
Known GenesSLC9A7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874717
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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