A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16178639



Internal ID6180455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35167207..35174665hg38UCSC Ensembl
chr20:33755010..33762468hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387459
hg197459
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645712
Supporting Variants
SamplesHG02050
Known GenesPROCR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16178639
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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