A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6183932



Internal ID8907831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9134840..9135996hg38UCSC Ensembl
chr19:9245516..9246672hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670511
Supporting Variants
SamplesHG00372
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6183932
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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