A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795896



Internal ID21241234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3393203..3393203hg38UCSC Ensembl
chr16:3443203..3443203hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682850, nssv13692253
Samples
Known GenesZSCAN32
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795896
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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