A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603432



Internal ID6990463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183065013..183067399hg38UCSC Ensembl
Innerchr4:183065163..183067249hg38UCSC Ensembl
Outerchr4:183064863..183067549hg38UCSC Ensembl
chr4:183986166..183988552hg19UCSC Ensembl
Innerchr4:183986316..183988402hg19UCSC Ensembl
Outerchr4:183986016..183988702hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382387
hg192387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11732267, essv11732268, essv11732263, essv11732260, essv11732258, essv11732269, essv11732265, essv11732264, essv11732266, essv11732262, essv11732261, essv11732259
SamplesHG03366, NA20298, NA19384, HG02968, HG03388, NA18523, HG02772, NA19108, HG03367, HG03103, HG02970, HG03072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603432
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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