A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093734



Internal ID21283637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31958834..31960882hg38UCSC Ensembl
Innerchr12:32111768..32113816hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg382049
hg192049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111672
Supporting Variants
Samplessample348
Known GenesKIAA1551
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093734
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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