A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6186293



Internal ID9163696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14400738..14402351hg38UCSC Ensembl
Outerchr19:14400701..14402401hg38UCSC Ensembl
Innerchr19:14511550..14513163hg19UCSC Ensembl
Outerchr19:14511513..14513213hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666679
Supporting Variants
SamplesHG01174
Known GenesCD97
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6186293
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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