A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205257



Internal ID21344059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101515356..101515356hg38UCSC Ensembl
chrX:100770343..100770343hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949735
Supporting Variants
SamplesHG002
Known GenesARMCX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205257
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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