A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1032656



Internal ID11849095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1327665..1327665hg38UCSC Ensembl
chr10:1369860..1369860hg19UCSC Ensembl
chr10:1359860..1359860hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3751506
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1032656
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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