A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2797940



Internal ID21243278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77456599..77456658hg38UCSC Ensembl
chr17:75452681..75452740hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681935
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2797940
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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