A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1628805



Internal ID12791925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10983175..10983912hg38UCSC Ensembl
chr1:11043232..11043969hg19UCSC Ensembl
chr1:10965819..10966556hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38738
hg19738
hg18738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3981893
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1628805
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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