A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205979



Internal ID21344783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22224947..22224947hg38UCSC Ensembl
chrX:22243064..22243064hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951336
Supporting Variants
SamplesHG002
Known GenesPHEX
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205979
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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