A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16996211



Internal ID64923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38195089..38197578hg38UCSC Ensembl
chr7:38234691..38237179hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382490
hg192489
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555872
Supporting Variants
Samples
Known GenesSTARD3NL
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16996211
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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