A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201878



Internal ID22351118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24169594..24170173hg38UCSC Ensembl
chrX:24187711..24188290hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350689
SamplesHG00731
Known GenesZFX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201878
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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