A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116178



Internal ID21299444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152643527..152645303hg38UCSC Ensembl
InnerchrX:151811988..151813764hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381777
hg191777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101771, nssv14101728
Samplessample359, sample321
Known GenesGABRQ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116178
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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