A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501920



Internal ID22559859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69348632..69351408hg38UCSC Ensembl
chr7:68813618..68816394hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg382777
hg192777
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501920
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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