A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704874



Internal ID21226679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107847457..107847513hg38UCSC Ensembl
chr7:107487902..107487958hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814685
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704874
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.95


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