A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643838



Internal ID6683907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18455241..18455855hg38UCSC Ensembl
Innerchr19:18455243..18455854hg38UCSC Ensembl
Outerchr19:18455240..18455857hg38UCSC Ensembl
chr19:18566051..18566665hg19UCSC Ensembl
Innerchr19:18566053..18566664hg19UCSC Ensembl
Outerchr19:18566050..18566667hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16003959, essv16003949, essv16003950, essv16003954, essv16003944, essv16003956, essv16003951, essv16003952, essv16003945, essv16003957, essv16003947, essv16003943, essv16003953, essv16003948, essv16003946, essv16003955, essv16003960, essv16003958
SamplesHG00096, NA12414, HG03607, NA20512, HG02792, HG01070, HG01168, NA20317, NA12044, NA20869, HG01048, NA20318, HG03775, HG03871, HG00110, HG02724, NA06985, NA20754
Known GenesELL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643838
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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