A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196702



Internal ID22346671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122371443..122371605hg38UCSC Ensembl
chrX:121505296..121505458hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352759
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196702
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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