A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086429



Internal ID21269845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121425566..121465100hg38UCSC Ensembl
Innerchr6:121746712..121786246hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3839535
hg1939535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112744
Supporting Variants
Samplessample143
Known GenesGJA1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086429
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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