A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3921631



Internal ID11840240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41361796..41362088hg38UCSC Ensembl
chr19:41867701..41867993hg19UCSC Ensembl
chr19:46559541..46559833hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38293
hg19293
hg18293
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1542493
Supporting Variants
SamplesHuRef
Known GenesB9D2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3921631
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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