A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107400



Internal ID6109216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57971972..57980802hg38UCSC Ensembl
chr19:58483340..58492170hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg388831
hg198831
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644917
Supporting Variants
SamplesHG03977
Known GenesC19orf18, ZNF606
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107400
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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