A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643791



Internal ID6683861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16149438..16170044hg38UCSC Ensembl
Innerchr19:16149438..16170044hg38UCSC Ensembl
Outerchr19:16149191..16170353hg38UCSC Ensembl
chr19:16260248..16280855hg19UCSC Ensembl
Innerchr19:16260248..16280855hg19UCSC Ensembl
Outerchr19:16260001..16281164hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3820607
hg1920608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002729
SamplesHG01577
Known GenesCIB3, HSH2D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643791
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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