A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218444



Internal ID20785484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15541961..15566252hg38UCSC Ensembl
chr7:15581586..15605877hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3824292
hg1924292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615633
Supporting Variants
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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