A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997959



Internal ID66181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67275319..67410698hg38UCSC Ensembl
chr7:66740306..66875685hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38135380
hg19135380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492990
Supporting Variants
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997959
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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