A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152288



Internal ID20719328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16337854..16417622hg38UCSC Ensembl
chr7:16377479..16457247hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3879769
hg1979769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610699
Supporting Variants
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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