A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114171



Internal ID21297437
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 StatusM
Merged Variantsdgv1259n145
Supporting Variantsnssv14104956, nssv14104135, nssv14101792
Samplessample380, sample140, sample81
Known GenesGPR64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114171
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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