A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151316



Internal ID20718356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103150208..103189912hg38UCSC Ensembl
chr7:102790655..102830359hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3839705
hg1939705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614142
Supporting Variants
Samples
Known GenesDPY19L2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151316
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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