A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3670605



Internal ID11744578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269690..77269763hg38UCSC Ensembl
chr14:77736033..77736106hg19UCSC Ensembl
chr14:76805786..76805859hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3874
hg1974
hg1874
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1739588
Supporting Variants
SamplesHuRef
Known GenesNGB
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3670605
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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