A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154638



Internal ID20721678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45098490..45101141hg38UCSC Ensembl
chr7:45138089..45140740hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382652
hg192652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619318
Supporting Variants
Samples
Known GenesTBRG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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