A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16220417



Internal ID6728099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61713674..61737698hg38UCSC Ensembl
chr20:60288730..60312754hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3824025
hg1924025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646276
Supporting Variants
SamplesNA20853
Known GenesCDH4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16220417
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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