A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15969665



Internal ID5971481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2901660..2914395hg38UCSC Ensembl
Innerchr19:2901708..2914347hg38UCSC Ensembl
Outerchr19:2901612..2914443hg38UCSC Ensembl
chr19:2901658..2914393hg19UCSC Ensembl
Innerchr19:2901706..2914345hg19UCSC Ensembl
Outerchr19:2901610..2914441hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812736
hg1912736
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643442
Supporting Variants
SamplesHG00120
Known GenesZNF57
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15969665
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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