A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16056067



Internal ID6057883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41443924..41501183hg38UCSC Ensembl
chr19:41949829..42007093hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3857260
hg1957265
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644380
Supporting Variants
SamplesNA19446
Known GenesC19orf69, LOC100505495
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16056067
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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