A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997498



Internal ID65874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52323929..52324491hg38UCSC Ensembl
chr7:52391625..52392187hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997498
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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