A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3949881



Internal ID11465305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32777616..32777616hg38UCSC Ensembl
chr15:33069817..33069817hg19UCSC Ensembl
chr15:30857109..30857109hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1210728
Supporting Variants
SamplesHuRef
Known GenesFMN1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3949881
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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