A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447837



Internal ID22505707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154785855..154785957hg38UCSC Ensembl
chrX:154014130..154014232hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5879606
Supporting Variants
Samples
Known GenesMPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447837
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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