A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5430446



Internal ID9226932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106566904..106569747hg38UCSC Ensembl
Outerchr10:106566867..106569797hg38UCSC Ensembl
Innerchr10:108326662..108329505hg19UCSC Ensembl
Outerchr10:108326625..108329555hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg382931
hg192931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665513
Supporting Variants
SamplesNA11892
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5430446
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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