A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6517449



Internal ID9494852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71416255..71421549hg38UCSC Ensembl
chr10:73176012..73181306hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385295
hg195295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672656
Supporting Variants
SamplesNA19716
Known GenesCDH23
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6517449
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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