A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104958



Internal ID21269621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:52798231..52934420hg38UCSC Ensembl
InnerchrX:52827271..52963629hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38136190
hg19136359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110949
Supporting Variants
Samplessample141
Known GenesFAM156A, FAM156B, XAGE3, XAGE5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104958
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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