A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228006



Internal ID20795046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55508315..55685753hg38UCSC Ensembl
chr7:55576008..55753446hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38177439
hg19177439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612532
Supporting Variants
Samples
Known GenesFKBP9L, VOPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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