A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001916



Internal ID7067034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:61489265..61490145hg38UCSC Ensembl
Outerchr3:61474939..61475819hg19UCSC Ensembl
Outerchr3:61449979..61450859hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38881
hg19881
hg18881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564899
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001916
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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