A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599851



Internal ID6986896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20765371..20767026hg38UCSC Ensembl
Innerchr4:20765383..20767014hg38UCSC Ensembl
Outerchr4:20765359..20767038hg38UCSC Ensembl
chr4:20766994..20768649hg19UCSC Ensembl
Innerchr4:20767006..20768637hg19UCSC Ensembl
Outerchr4:20766982..20768661hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11367190
SamplesNA20858
Known GenesKCNIP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599851
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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