A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602566



Internal ID6989599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145832703..145838215hg38UCSC Ensembl
Innerchr4:145832753..145838165hg38UCSC Ensembl
Outerchr4:145832653..145838265hg38UCSC Ensembl
chr4:146753855..146759367hg19UCSC Ensembl
Innerchr4:146753905..146759317hg19UCSC Ensembl
Outerchr4:146753805..146759417hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg385513
hg195513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11642157, essv11642161, essv11642163, essv11642160, essv11642152, essv11642153, essv11642155, essv11642154, essv11642156, essv11642159, essv11642158, essv11642162
SamplesNA19704, HG03963, NA18988, NA19068, HG02786, NA18868, NA19317, NA18986, NA19000, HG03646, NA18989, HG03955
Known GenesZNF827
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602566
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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