A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708980



Internal ID21230766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62705306..62705619hg38UCSC Ensembl
chr9:47016607..47016920hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708980
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0384615


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