A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010744



Internal ID7074695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:15825436..15831614hg38UCSC Ensembl
Outerchr1:16151931..16158109hg19UCSC Ensembl
Outerchr1:16024518..16030696hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg386179
hg196179
hg186179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564107
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010744
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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