A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3983782



Internal ID11778091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36287072..36287072hg38UCSC Ensembl
chr11:36308622..36308622hg19UCSC Ensembl
chr11:36265198..36265198hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38416
hg19416
hg18416
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1531905
Supporting Variants
SamplesHuRef
Known GenesCOMMD9
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3983782
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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