A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4086483



Internal ID11675392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92471927..92472247hg38UCSC Ensembl
chr4:93393078..93393398hg19UCSC Ensembl
chr4:93612101..93612421hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38321
hg19321
hg18321
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1428298
Supporting Variants
SamplesHuRef
Known GenesGRID2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4086483
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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