A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6551205



Internal ID9073277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19972164..20577431hg38UCSC Ensembl
Outerchr19:19972130..20577466hg38UCSC Ensembl
Innerchr19:20082973..20760237hg19UCSC Ensembl
Outerchr19:20082939..20760272hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38605337
hg19677334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676413
Supporting Variants
SamplesHG01047
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)essv6551205
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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