A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156728



Internal ID20723768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1927501..1979900hg38UCSC Ensembl
chr7:1967137..2019535hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3852400
hg1952399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608727
Supporting Variants
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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