A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476473



Internal ID22534371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77722148..77724247hg38UCSC Ensembl
chr17:75718230..75720329hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877370
Supporting Variants
Samples
Known GenesLOC100132174
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476473
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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