A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863619



Internal ID3865435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74215304..74288876hg38UCSC Ensembl
chr10:75975062..76048634hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3873573
hg1973573
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623826
Supporting Variants
SamplesHG00141
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863619
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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