A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113585



Internal ID21296851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:120135236..120138689hg38UCSC Ensembl
InnerchrX:119269146..119272596hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg383454
hg193451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104116, nssv14104120, nssv14104944
Samplessample70, sample130, sample61
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113585
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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