A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107462



Internal ID3229789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58220865..58254049hg38UCSC Ensembl
Innerchr19:58221365..58253549hg38UCSC Ensembl
Outerchr19:58219865..58255049hg38UCSC Ensembl
chr19:58732231..58765415hg19UCSC Ensembl
Innerchr19:58732731..58764915hg19UCSC Ensembl
Outerchr19:58731231..58766415hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3833185
hg1933185
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644928
Supporting Variants
SamplesHG02839
Known GenesZNF544
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107462
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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