A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154021



Internal ID20721061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149259089..149315146hg38UCSC Ensembl
chr7:148956180..149012237hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3856058
hg1956058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428767
Supporting Variants
Samples
Known GenesLOC155060, ZNF783
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154021
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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