A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446331



Internal ID22504201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9979891..9987076hg38UCSC Ensembl
chr6:9980124..9987309hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg387186
hg197186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891681
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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