A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987776



Internal ID7075274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99909938..99910786hg38UCSC Ensembl
chr3:99628782..99629630hg19UCSC Ensembl
chr3:101111472..101112320hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38849
hg19849
hg18849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574963
SamplesHuRef
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987776
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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