A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525532



Internal ID22394910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119900344..119924648hg38UCSC Ensembl
chrX:119034307..119058611hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3824305
hg1924305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352696, nssv14352695
SamplesNA19239, NA19240
Known GenesAKAP14
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525532
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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