A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155001



Internal ID20722041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2442501..2443059hg38UCSC Ensembl
chr7:2482136..2482694hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600510
Supporting Variants
Samples
Known GenesLOC101927181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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