A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3833922



Internal ID11927949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38485067..38485067hg38UCSC Ensembl
chr1:38950739..38950739hg19UCSC Ensembl
chr1:38723326..38723326hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1309666
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3833922
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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