A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6014568



Internal ID9725210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29676999..29682946hg38UCSC Ensembl
Outerchr19:29676962..29682996hg38UCSC Ensembl
Innerchr19:30167906..30173853hg19UCSC Ensembl
Outerchr19:30167869..30173903hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg386035
hg196035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659627
Supporting Variants
SamplesNA19625
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6014568
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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