A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796673



Internal ID21242011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29895264..29895264hg38UCSC Ensembl
chr17:28222282..28222282hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694065
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796673
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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