A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101671



Internal ID21279689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:11428850..11430494hg38UCSC Ensembl
InnerchrX:11446970..11448614hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381645
hg191645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110370
Supporting Variants
Samplessample287
Known GenesARHGAP6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101671
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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