A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218566



Internal ID20785606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97839701..97845300hg38UCSC Ensembl
chr7:97469013..97474612hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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