A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644387



Internal ID7031142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41552950..41555787hg38UCSC Ensembl
Innerchr19:41552958..41555780hg38UCSC Ensembl
Outerchr19:41552943..41555795hg38UCSC Ensembl
chr19:42059320..42062157hg19UCSC Ensembl
Innerchr19:42059328..42062150hg19UCSC Ensembl
Outerchr19:42059313..42062165hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382838
hg192838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16056132, essv16056128, essv16056126, essv16056122, essv16056133, essv16056131, essv16056127, essv16056129, essv16056123, essv16056130, essv16056125, essv16056124
SamplesHG01773, NA20813, NA07048, HG00139, HG01628, HG01519, NA11994, HG01603, NA20828, HG00258, HG01489, HG00259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644387
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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