A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349885



Internal ID22206878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12744294..12744393hg38UCSC Ensembl
chrX:12762413..12762512hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526943
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349885
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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