A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156784



Internal ID20723824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19720501..19721800hg38UCSC Ensembl
chr7:19760124..19761423hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612032
Supporting Variants
Samples
Known GenesTMEM196
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00078


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