A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3608878



Internal ID12152990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186292815..186293598hg38UCSC Ensembl
chr4:187213969..187214752hg19UCSC Ensembl
chr4:187450963..187451746hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38784
hg19784
hg18784
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1700178
Supporting Variants
SamplesHuRef
Known GenesF11-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3608878
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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