A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151957



Internal ID20718997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104129286..104130727hg38UCSC Ensembl
chr7:103769733..103771174hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615671
Supporting Variants
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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