A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101654



Internal ID21278942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:54529031..54532535hg38UCSC Ensembl
InnerchrX:54555464..54558968hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg383505
hg193505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110656
Supporting Variants
Samplessample275
Known GenesGNL3L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101654
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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