A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993647



Internal ID63221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10501968..10748037hg38UCSC Ensembl
chr7:10541595..10787664hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38246070
hg19246070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993647
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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