A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4013785



Internal ID11748088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10507915..10507966hg38UCSC Ensembl
chr3:10549599..10549650hg19UCSC Ensembl
chr3:10524599..10524650hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1720167
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4013785
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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