A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205655



Internal ID21344458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:31352199..31352199hg38UCSC Ensembl
chrX:31370316..31370316hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925636
Supporting Variants
SamplesHG002
Known GenesDMD
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205655
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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