A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380805



Internal ID22438675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76563878..76564216hg38UCSC Ensembl
chr17:74559960..74560298hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930720
Supporting Variants
Samples
Known GenesSNHG16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380805
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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