A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644266



Internal ID6684334
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660e214
Supporting Variantsessv16049696, essv16049697, essv16049698
SamplesHG01947, NA19456, NA19327
Known GenesZNF461, ZNF567, ZNF850
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644266
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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