A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4103839



Internal ID11658036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154378944..154379264hg38UCSC Ensembl
chr3:154096733..154097053hg19UCSC Ensembl
chr3:155579427..155579747hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38321
hg19321
hg18321
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1340831
Supporting Variants
SamplesHuRef
Known GenesGPR149
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4103839
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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