A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222085



Internal ID20789125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112211150..112248901hg38UCSC Ensembl
chr7:111851205..111888956hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3837752
hg1937752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600975
Supporting Variants
Samples
Known GenesZNF277
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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