A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15991636



Internal ID5993452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11931658..11932390hg38UCSC Ensembl
Innerchr19:11931658..11932390hg38UCSC Ensembl
Outerchr19:11931451..11932579hg38UCSC Ensembl
chr19:12042473..12043205hg19UCSC Ensembl
Innerchr19:12042473..12043205hg19UCSC Ensembl
Outerchr19:12042266..12043394hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643686
Supporting Variants
SamplesHG03114
Known GenesZNF700
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15991636
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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