A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6031374



Internal ID9665789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23412219..23419418hg38UCSC Ensembl
chr10:23701148..23708347hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671532
Supporting Variants
SamplesNA19396
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6031374
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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