A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3889150



Internal ID11526035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1327812..1327812hg38UCSC Ensembl
chr10:1370007..1370007hg19UCSC Ensembl
chr10:1360007..1360007hg18UCSC 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 Variantsesv1309284
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3889150
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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