A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105062



Internal ID21274934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:30299446..30304662hg38UCSC Ensembl
InnerchrX:30317563..30322779hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg385217
hg195217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117134
Supporting Variants
Samplessample214
Known GenesNR0B1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105062
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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