A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597167



Internal ID6984481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100060963..100098910hg38UCSC Ensembl
chr3:99779807..99817754hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3837948
hg1937948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv916e214
Supporting Variantsessv11083885, essv11083886
SamplesNA21129, HG03940
Known GenesCMSS1, FILIP1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597167
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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