A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167166



Internal ID21487721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31569662..31569662hg38UCSC Ensembl
chrX:31587779..31587779hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614371
Supporting Variants
SamplesNA18534
Known GenesDMD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167166
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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