A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599949



Internal ID6640211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24809012..24810524hg38UCSC Ensembl
Innerchr4:24809028..24810508hg38UCSC Ensembl
Outerchr4:24808996..24810540hg38UCSC Ensembl
chr4:24810634..24812146hg19UCSC Ensembl
Innerchr4:24810650..24812130hg19UCSC Ensembl
Outerchr4:24810618..24812162hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370676
SamplesNA19475
Known GenesCCDC149
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599949
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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