A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469008



Internal ID22526898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31600481..31600544hg38UCSC Ensembl
chrX:31618598..31618661hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870649
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469008
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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