A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524971



Internal ID22394346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136278563..136278892hg38UCSC Ensembl
chrX:135360722..135361051hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354347, nssv14354345, nssv14354348, nssv14354346, nssv14354349
SamplesHG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524971
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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