A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516145



Internal ID22574107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:32712564..32719698hg38UCSC Ensembl
chrX:32730681..32737815hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg387135
hg197135
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5969636
Supporting Variants
Samples
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516145
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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