A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6589638



Internal ID9567041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74292681..74293597hg38UCSC Ensembl
chr10:76052439..76053355hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661407
Supporting Variants
SamplesHG00179
Known GenesADK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6589638
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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