A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709396



Internal ID21231174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16197509..16198725hg38UCSC Ensembl
chr7:16237134..16238350hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816476
Supporting Variants
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709396
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.328125


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