A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154217



Internal ID20721257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2174976..2222943hg38UCSC Ensembl
chr7:2214611..2262578hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3847968
hg1947968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618771
Supporting Variants
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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