A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11655527



Internal ID6901889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153023297..153025582hg38UCSC Ensembl
Innerchr4:153023306..153025574hg38UCSC Ensembl
Outerchr4:153023289..153025591hg38UCSC Ensembl
chr4:153944449..153946734hg19UCSC Ensembl
Innerchr4:153944458..153946726hg19UCSC Ensembl
Outerchr4:153944441..153946743hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382286
hg192286
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602717
Supporting Variants
SamplesNA21110
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11655527
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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