A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4061490



Internal ID11353698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89328784..89328784hg38UCSC Ensembl
chr16:89395192..89395192hg19UCSC Ensembl
chr16:87922693..87922693hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1704981
Supporting Variants
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4061490
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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