A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694698



Internal ID21216560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63488530..63488530hg38UCSC Ensembl
chr17:61565891..61565891hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797831
Supporting Variants
Samples
Known GenesACE
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.532258


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