A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3808532



Internal ID11606653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33218675..33218675hg38UCSC Ensembl
chr19:33709581..33709581hg19UCSC Ensembl
chr19:38401421..38401421hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38115
hg19115
hg18115
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1069310
Supporting Variants
SamplesHuRef
Known GenesSLC7A10
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3808532
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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