A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6465751



Internal ID9443154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1423568..1423768hg38UCSC Ensembl
chr10:1465763..1465963hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666228
Supporting Variants
SamplesHG01173
Known GenesADARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6465751
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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