A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053969



Internal ID20621009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17310780..17310917hg38UCSC Ensembl
chr1:17637275..17637412hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325032
Supporting Variants
Samples
Known GenesPADI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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