A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700086



Internal ID21221919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40752822..40752822hg38UCSC Ensembl
chr4:40754839..40754839hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810272
Supporting Variants
Samples
Known GenesNSUN7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700086
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.78125


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