A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623092



Internal ID6663260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45465942..45485335hg38UCSC Ensembl
chr10:45961390..45980783hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3819394
hg1919394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13770334
SamplesHG03380
Known GenesMARCH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623092
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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