A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3891525



Internal ID11870346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32581187..32581187hg38UCSC Ensembl
chr1:33046788..33046788hg19UCSC Ensembl
chr1:32819375..32819375hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38611
hg19611
hg18611
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1277305
Supporting Variants
SamplesHuRef
Known GenesZBTB8A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3891525
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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