A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643690



Internal ID7030449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12006494..12014300hg38UCSC Ensembl
Innerchr19:12006503..12014291hg38UCSC Ensembl
Outerchr19:12006485..12014309hg38UCSC Ensembl
chr19:12117309..12125115hg19UCSC Ensembl
Innerchr19:12117318..12125106hg19UCSC Ensembl
Outerchr19:12117300..12125124hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387807
hg197807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15991874
SamplesHG02660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643690
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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