A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3981893



Internal ID11779979
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1628805
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3981893
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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