A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101728



Internal ID21282122
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 StatusS
Merged Variantsnsv3116178
Supporting Variants
Samplessample321
Known GenesGABRQ
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101728
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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