A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599625



Internal ID6639889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10478051..10496566hg38UCSC Ensembl
Innerchr4:10478051..10496566hg38UCSC Ensembl
Outerchr4:10477551..10497066hg38UCSC Ensembl
chr4:10479675..10498190hg19UCSC Ensembl
Innerchr4:10479675..10498190hg19UCSC Ensembl
Outerchr4:10479175..10498690hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3818516
hg1918516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11355319
SamplesNA18510
Known GenesCLNK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599625
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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