A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456317



Internal ID22514194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32714522..32721578hg38UCSC Ensembl
chrX:32732639..32739695hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg387057
hg197057
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873381
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456317
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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