A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439058



Internal ID22496928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29577250..29584977hg38UCSC Ensembl
chr6:29545027..29552754hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387728
hg197728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896529
Supporting Variants
Samples
Known GenesSNORD32B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439058
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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