A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526218



Internal ID22395598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121172376..121172473hg38UCSC Ensembl
chrX:120306230..120306327hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10265n152
Supporting Variantsnssv14352740, nssv14352739
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526218
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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