A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502751



Internal ID22560692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73335615..73339525hg38UCSC Ensembl
chr7:72749617..72753528hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383911
hg193912
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860998
Supporting Variants
Samples
Known GenesFKBP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502751
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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