A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3328729



Internal ID15175716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3761997..3762016hg38UCSC Ensembl
Innerchr19:3761993..3762020hg38UCSC Ensembl
Outerchr19:3761974..3762039hg38UCSC Ensembl
chr19:3761995..3762014hg19UCSC Ensembl
Innerchr19:3761991..3762018hg19UCSC Ensembl
Outerchr19:3761972..3762037hg19UCSC Ensembl
chr19:3712995..3713014hg18UCSC Ensembl
Innerchr19:3713018..3712991hg18UCSC Ensembl
Outerchr19:3712972..3713037hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8678311
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3328729
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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