A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475914



Internal ID22533812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74977234..74984504hg38UCSC Ensembl
chr17:72973329..72980599hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg387271
hg197271
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475914
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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