A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv630e199



Internal ID22758403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19963492..20577466hg38UCSC Ensembl
chr19:20074301..20760272hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38613975
hg19685972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2676413, esv2673357
SamplesHG00231, HG00148, HG01047, HG01102
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv630e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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