A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994900



Internal ID64031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24287238..24366474hg38UCSC Ensembl
chr7:24326857..24406093hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3879237
hg1979237
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562051
Supporting Variants
Samples
Known GenesNPY
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994900
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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