A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602652



Internal ID6989685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150128011..150132193hg38UCSC Ensembl
Innerchr4:150128013..150132192hg38UCSC Ensembl
Outerchr4:150128010..150132195hg38UCSC Ensembl
chr4:151049163..151053345hg19UCSC Ensembl
Innerchr4:151049165..151053344hg19UCSC Ensembl
Outerchr4:151049162..151053347hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg384183
hg194183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11651713, essv11651717, essv11651715, essv11651721, essv11651718, essv11651722, essv11651719, essv11651714, essv11651716, essv11651720
SamplesHG03280, NA18489, NA19921, HG02570, HG03159, HG01323, HG03567, HG02010, HG02971, NA19214
Known GenesDCLK2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602652
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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