A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6394117



Internal ID9371520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30462793..30462958hg38UCSC Ensembl
chr19:30953700..30953865hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662362
Supporting Variants
SamplesNA19064
Known GenesZNF536
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6394117
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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