A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3982155



Internal ID11779718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9923340..9923435hg38UCSC Ensembl
chr18:9923337..9923432hg19UCSC Ensembl
chr18:9913337..9913432hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3896
hg1996
hg1896
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1026283
Supporting Variants
SamplesHuRef
Known GenesVAPA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3982155
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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