A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421237



Internal ID22479107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160775991..160809077hg38UCSC Ensembl
chr6:161197023..161230109hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3833087
hg1933087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889075
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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