A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798806



Internal ID21244144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58863527..58863527hg38UCSC Ensembl
chr18:56530759..56530759hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709012
Samples
Known GenesZNF532
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798806
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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