A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083518



Internal ID21276665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112197788..112211571hg38UCSC Ensembl
Innerchr6:112518990..112532772hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3813784
hg1913783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116785
Supporting Variants
Samplessample24
Known GenesLAMA4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083518
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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