A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509295



Internal ID22567245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73311061..73370672hg38UCSC Ensembl
chr7:72725056..72784667hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3859612
hg1959612
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858601
Supporting Variants
Samples
Known GenesFKBP6, TRIM50
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509295
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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