A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526634



Internal ID22396016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45434811..45434872hg38UCSC Ensembl
chrX:45294056..45294117hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350437, nssv14351055, nssv14350438, nssv14351058, nssv14351057, nssv14351056
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526634
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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