A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6545512



Internal ID9522915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57216301..57219125hg38UCSC Ensembl
Outerchr19:57216264..57219175hg38UCSC Ensembl
Innerchr19:57727669..57730493hg19UCSC Ensembl
Outerchr19:57727632..57730543hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382912
hg192912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663783
Supporting Variants
SamplesNA20790
Known GenesZNF264
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6545512
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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