A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6005027



Internal ID8982430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29423216..29423791hg38UCSC Ensembl
chr10:29712145..29712720hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2677009
Supporting Variants
SamplesHG00247
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6005027
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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