A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101792



Internal ID21285955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:19072835..19075135hg38UCSC Ensembl
InnerchrX:19090953..19093253hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114171
Supporting Variants
Samplessample380
Known GenesGPR64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101792
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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