A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415797



Internal ID15262756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12018110..12018121hg38UCSC Ensembl
Innerchr19:12018089..12018142hg38UCSC Ensembl
Outerchr19:12018078..12018153hg38UCSC Ensembl
chr19:12128925..12128936hg19UCSC Ensembl
Innerchr19:12128904..12128957hg19UCSC Ensembl
Outerchr19:12128893..12128968hg19UCSC Ensembl
chr19:11989925..11989936hg18UCSC Ensembl
Innerchr19:11989957..11989904hg18UCSC Ensembl
Outerchr19:11989893..11989968hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7866077
SamplesNA12005
Known GenesZNF433
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415797
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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