A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161808



Internal ID20728848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93621672..93622308hg38UCSC Ensembl
chr7:93250984..93251620hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161808
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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