A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998373



Internal ID66461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74211662..74213572hg38UCSC Ensembl
chr7:73625992..73627902hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381911
hg191911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480342
Supporting Variants
Samples
Known GenesLAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998373
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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