A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106981



Internal ID20674021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105458901..105462900hg38UCSC Ensembl
chr4:106380058..106384057hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393165
Supporting Variants
Samples
Known GenesPPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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