A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525662



Internal ID22395040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132610869..132611296hg38UCSC Ensembl
chrX:131744897..131745324hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354274, nssv14354273
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525662
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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