A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665276



Internal ID9931381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21082696..21397596hg38UCSC Ensembl
Outerchr19:21082662..21397631hg38UCSC Ensembl
Innerchr19:21265502..21580398hg19UCSC Ensembl
Outerchr19:21265468..21580433hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38314970
hg19314966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6170831
SamplesNA20755
Known GenesZNF431, ZNF493, ZNF708, ZNF714, ZNF738
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665276
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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