A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6147715



Internal ID9125118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8147543..8148091hg38UCSC Ensembl
Outerchr19:8147506..8148141hg38UCSC Ensembl
Innerchr19:8212427..8212975hg19UCSC Ensembl
Outerchr19:8212390..8213025hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677615
Supporting Variants
SamplesNA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6147715
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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