A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15999977



Internal ID5774944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15553571..15566313hg38UCSC Ensembl
Innerchr19:15553581..15566303hg38UCSC Ensembl
Outerchr19:15553561..15566323hg38UCSC Ensembl
chr19:15664382..15677124hg19UCSC Ensembl
Innerchr19:15664392..15677114hg19UCSC Ensembl
Outerchr19:15664372..15677134hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3812743
hg1912743
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643770
Supporting Variants
SamplesNA19144
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15999977
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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