A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3644771



Internal ID12117097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49701858..49701858hg38UCSC Ensembl
chr19:50205115..50205115hg19UCSC Ensembl
chr19:54896927..54896927hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38439
hg19439
hg18439
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1209349
Supporting Variants
SamplesHuRef
Known GenesCPT1C
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3644771
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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