A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004637



Internal ID7069733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:65908206..65919037hg38UCSC Ensembl
Outerchr10:67667964..67678795hg19UCSC Ensembl
Outerchr10:67337970..67348801hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810832
hg1910832
hg1810832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564519
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004637
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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