A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978270



Internal ID20545310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116632541..116634113hg38UCSC Ensembl
chr10:118392052..118393624hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381573
hg191573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442523
Supporting Variants
Samples
Known GenesPNLIPRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978270
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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