A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13770336



Internal ID3772152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45494741..45532253hg38UCSC Ensembl
chr10:45990189..46027701hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3837513
hg1937513
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623094
Supporting Variants
SamplesHG03380
Known GenesMARCH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13770336
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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