A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6104975



Internal ID9588617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21862627..21872268hg38UCSC Ensembl
chr10:22151556..22161197hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389642
hg199642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669848
Supporting Variants
SamplesNA19198
Known GenesDNAJC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6104975
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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