A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994621



Internal ID63850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28911012..28911780hg38UCSC Ensembl
chr7:28950629..28951397hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994621
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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