A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790073



Internal ID21235411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43181882..43181882hg38UCSC Ensembl
chr10:43677330..43677330hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg381437
hg191437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706815
Samples
Known GenesCSGALNACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790073
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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