A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13823636



Internal ID1758513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56359827..56399977hg38UCSC Ensembl
chr10:58119588..58159738hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3840151
hg1940151
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623382
Supporting Variants
SamplesHG01620
Known GenesZWINT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13823636
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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