A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4337086



Internal ID11272938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1327765..1327765hg38UCSC Ensembl
chr10:1369960..1369960hg19UCSC Ensembl
chr10:1359960..1359960hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1537660
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4337086
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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