A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5759932



Internal ID8853509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37418845..37422300hg38UCSC Ensembl
chr17:35778929..35782406hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383456
hg193478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664726
Supporting Variants
SamplesHG00309
Known GenesTADA2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5759932
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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