A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13975585



Internal ID6128858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130541074..130566230hg38UCSC Ensembl
chr10:132339338..132364494hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3825157
hg1925157
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624939
Supporting Variants
SamplesNA19663
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13975585
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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