A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159561



Internal ID20726601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7483801..7484500hg38UCSC Ensembl
chr7:7523432..7524131hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609297
Supporting Variants
Samples
Known GenesCOL28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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