A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13796746



Internal ID2542412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49543320..49557226hg38UCSC Ensembl
chr10:50751366..50765272hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3813907
hg1913907
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623173
Supporting Variants
SamplesHG02259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13796746
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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