A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151338



Internal ID20718378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103459146..103465521hg38UCSC Ensembl
chr7:103099593..103105968hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386376
hg196376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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