A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476434



Internal ID22534332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75483217..75500593hg38UCSC Ensembl
chr17:73479298..73496674hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3817377
hg1917377
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883861
Supporting Variants
Samples
Known GenesCASKIN2, KIAA0195, MIR6785
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476434
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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