A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6117771



Internal ID9095174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:938037..938669hg38UCSC Ensembl
chr1:873417..874049hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663451
Supporting Variants
SamplesNA18544
Known GenesSAMD11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6117771
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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