A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13956579



Internal ID5460295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122602807..122624657hg38UCSC Ensembl
chr10:124362323..124384173hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3821851
hg1921851
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624781
Supporting Variants
SamplesNA18969
Known GenesDMBT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13956579
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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