A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235915



Internal ID20802955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75156101..75158300hg38UCSC Ensembl
chr7:74571907..74574106hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618917
Supporting Variants
Samples
Known GenesNCF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00034


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