A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3915475



Internal ID11499710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3145603..3145603hg38UCSC Ensembl
chr19:3145601..3145601hg19UCSC Ensembl
chr19:3096601..3096601hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38499
hg19499
hg18499
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1660661
Supporting Variants
SamplesHuRef
Known GenesGNA15
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3915475
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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