A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599439



Internal ID6986486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3895736..4169659hg38UCSC Ensembl
Innerchr4:3896236..4169159hg38UCSC Ensembl
Outerchr4:3894736..4170659hg38UCSC Ensembl
chr4:3897463..4171386hg19UCSC Ensembl
Innerchr4:3897963..4170886hg19UCSC Ensembl
Outerchr4:3896463..4172386hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38273924
hg19273924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11317808, essv11317799, essv11317805, essv11317807, essv11317803, essv11317802, essv11317800, essv11317798, essv11317806, essv11317801, essv11317804
SamplesHG03559, HG02891, HG02485, NA19917, HG01444, NA19473, HG03157, HG03896, NA20528, HG03303, HG03265
Known GenesFAM86EP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599439
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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