A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807933



Internal ID21253271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136893181..136893181hg38UCSC Ensembl
chr3:136612023..136612023hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691449
Samples
Known GenesNCK1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807933
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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