A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709012



Internal ID21230795
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 StatusS
Merged Variantsnsv2798806
Supporting Variants
Samples
Known GenesZNF532
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709012
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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