A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644623



Internal ID6684689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49417657..49422388hg38UCSC Ensembl
Innerchr19:49417672..49422374hg38UCSC Ensembl
Outerchr19:49417643..49422403hg38UCSC Ensembl
chr19:49920914..49925645hg19UCSC Ensembl
Innerchr19:49920929..49925631hg19UCSC Ensembl
Outerchr19:49920900..49925660hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg384732
hg194732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16075213
SamplesNA12815
Known GenesCCDC155
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644623
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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