A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3633549



Internal ID12128319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34631159..34632164hg38UCSC Ensembl
chr14:35100365..35101370hg19UCSC Ensembl
chr14:34170116..34171121hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381006
hg191006
hg181006
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1132950
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3633549
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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