A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1300014



Internal ID12463136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23429600..23429600hg38UCSC Ensembl
chr10:23718529..23718529hg19UCSC Ensembl
chr10:23758535..23758535hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3717212
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1300014
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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