A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205222



Internal ID21344022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65457303..65457303hg38UCSC Ensembl
chrX:64677183..64677183hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929002
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205222
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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