A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995700



Internal ID64570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:53187133..53197454hg38UCSC Ensembl
chr7:53254826..53265147hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3810322
hg1910322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995700
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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