A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223499



Internal ID20790539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149408401..149486200hg38UCSC Ensembl
chr7:149105492..149183291hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3877800
hg1977800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420257
Supporting Variants
Samples
Known GenesZNF746, ZNF777
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223499
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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