A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13956039



Internal ID6896463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122584915..122593721hg38UCSC Ensembl
chr10:124344431..124353237hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388807
hg198807
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624777
Supporting Variants
SamplesNA21108
Known GenesDMBT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13956039
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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