A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4029516



Internal ID11385672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35297713..35298149hg38UCSC Ensembl
chr19:35788616..35789052hg19UCSC Ensembl
chr19:40480456..40480892hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38437
hg19437
hg18437
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1763084
Supporting Variants
SamplesHuRef
Known GenesMAG
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4029516
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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