A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366486



Internal ID22592155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72291551..72291999hg38UCSC Ensembl
chr10:74051309..74051757hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918952
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366486
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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