A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789265



Internal ID21234603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70220597..70220666hg38UCSC Ensembl
chr10:71980353..71980422hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692551
Samples
Known GenesPPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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