A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623206



Internal ID6663374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50507424..50513989hg38UCSC Ensembl
chr10:52267184..52273749hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg386566
hg196566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128e214
Supporting Variantsessv13803070, essv13803069
SamplesNA21133, HG03931
Known GenesSGMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623206
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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