A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101820



Internal ID21287041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140958061..140994724hg38UCSC Ensembl
InnerchrX:140040226..140076889hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3836664
hg1936664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113356
Supporting Variants
Samplessample397
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101820
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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