A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3945141



Internal ID11816731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66522260..66522309hg38UCSC Ensembl
chr5:65818088..65818137hg19UCSC Ensembl
chr5:65853844..65853893hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1607767
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3945141
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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