A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3978193



Internal ID11783680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186433366..186433780hg38UCSC Ensembl
chr4:187354520..187354934hg19UCSC Ensembl
chr4:187591514..187591928hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38415
hg19415
hg18415
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1681070
Supporting Variants
SamplesHuRef
Known GenesF11-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3978193
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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