A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2816476



Internal ID21261814
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 StatusM
Merged Variants
Supporting Variantsnssv13709396
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2816476
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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