A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646262



Internal ID7033007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61401111..61419732hg38UCSC Ensembl
Innerchr20:61401111..61419732hg38UCSC Ensembl
Outerchr20:61400611..61420232hg38UCSC Ensembl
chr20:59976167..59994788hg19UCSC Ensembl
Innerchr20:59976167..59994788hg19UCSC Ensembl
Outerchr20:59975667..59995288hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3818622
hg1918622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16219872
SamplesHG02725
Known GenesCDH4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646262
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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