A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4325077



Internal ID11260929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79558577..79558661hg38UCSC Ensembl
chr4:80479731..80479815hg19UCSC Ensembl
chr4:80698755..80698839hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3885
hg1985
hg1885
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1181170
Supporting Variants
SamplesHuRef
Known GenesLINC00989
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4325077
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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