A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6361641



Internal ID9339044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54051962..54057368hg38UCSC Ensembl
Outerchr19:54051591..54058038hg38UCSC Ensembl
Innerchr19:54555216..54560622hg19UCSC Ensembl
Outerchr19:54554845..54561292hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386448
hg196448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665514
Supporting Variants
SamplesNA18934
Known GenesVSTM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6361641
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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