A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004778



Internal ID70824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149089736..149092853hg38UCSC Ensembl
chr7:148786828..148789945hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg383118
hg193118
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556600
Supporting Variants
Samples
Known GenesZNF786
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004778
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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