A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476522



Internal ID22534420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81616648..81619390hg38UCSC Ensembl
chr17:79583674..79586416hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382743
hg192743
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881542
Supporting Variants
Samples
Known GenesNPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476522
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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