A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699729



Internal ID21221563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75254683..75254766hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2815630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699729
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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