A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998955



Internal ID66878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84051236..84056021hg38UCSC Ensembl
chr7:83680552..83685337hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg384786
hg194786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142298
Supporting Variants
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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