A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16107250



Internal ID6109066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57476961..57491649hg38UCSC Ensembl
chr19:57988329..58003017hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3814689
hg1914689
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644903
Supporting Variants
SamplesNA20889
Known GenesZNF419, ZNF772
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16107250
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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