A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16049697



Internal ID6051513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36632108..36747345hg38UCSC Ensembl
chr19:37123010..37238247hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38115238
hg19115238
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644266
Supporting Variants
SamplesNA19327
Known GenesZNF461, ZNF567, ZNF850
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16049697
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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