A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4171093



Internal ID11106945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88912221..88912273hg38UCSC Ensembl
chr4:89833372..89833424hg19UCSC Ensembl
chr4:90052395..90052447hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1054095
Supporting Variants
SamplesHuRef
Known GenesFAM13A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4171093
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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