A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3968585



Internal ID11793287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33757389..33757464hg38UCSC Ensembl
chr19:34248294..34248369hg19UCSC Ensembl
chr19:38940134..38940209hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1416262
Supporting Variants
SamplesHuRef
Known GenesCHST8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3968585
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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