A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3763691



Internal ID11998179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85604774..85604774hg38UCSC Ensembl
chr16:85638380..85638380hg19UCSC Ensembl
chr16:84195881..84195881hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38124
hg19124
hg18124
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1101106
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3763691
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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