A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068669



Internal ID20635709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14975801..14976700hg38UCSC Ensembl
chr21:16348122..16349021hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537628
Supporting Variants
Samples
Known GenesNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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