A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3766837



Internal ID11648348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37242106..37242106hg38UCSC Ensembl
chr19:37733008..37733008hg19UCSC Ensembl
chr19:42424848..42424848hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1570552
Supporting Variants
SamplesHuRef
Known GenesZNF383
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3766837
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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