A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv660e214



Internal ID20122083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36630846..36747345hg38UCSC Ensembl
chr19:37121748..37238247hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38116500
hg19116500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644266, esv3644265
SamplesHG01947, NA19456, NA19327
Known GenesZNF461, ZNF567, ZNF850
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv660e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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