A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5938914



Internal ID9684382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74139536..74143073hg38UCSC Ensembl
Outerchr10:74139499..74143123hg38UCSC Ensembl
Innerchr10:75899294..75902831hg19UCSC Ensembl
Outerchr10:75899257..75902881hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383625
hg193625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658956
Supporting Variants
SamplesNA19435
Known GenesAP3M1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5938914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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