A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705770



Internal ID21227568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96404923..96405253hg38UCSC Ensembl
chr6:96852799..96853129hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813897
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705770
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.859375


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