A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3833382



Internal ID11928489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997825..166997825hg38UCSC Ensembl
chr6:167411313..167411313hg19UCSC Ensembl
chr6:167331303..167331303hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381552
hg191552
hg181552
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1673761
Supporting Variants
SamplesHuRef
Known GenesMIR3939
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3833382
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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