A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525557



Internal ID22394935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38496985..38497635hg38UCSC Ensembl
chrX:38356238..38356888hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351767, nssv14351766
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525557
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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