A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv916e214



Internal ID22756810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100060429..100098910hg38UCSC Ensembl
chr3:99779273..99817754hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3838482
hg1938482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597167, esv3597166
SamplesNA21110, NA21129, HG03940
Known GenesCMSS1, FILIP1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv916e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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