A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701268



Internal ID21223097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101509188..101509188hg38UCSC Ensembl
chr8:102521416..102521416hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817143
Supporting Variants
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701268
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.65625


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