A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5939624



Internal ID8917027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9161898..9162015hg38UCSC Ensembl
chr17:9065215..9065332hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675061
Supporting Variants
SamplesNA19651
Known GenesNTN1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5939624
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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