A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427062



Internal ID22484932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106580154..106580234hg38UCSC Ensembl
chr6:107028029..107028109hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888894
Supporting Variants
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427062
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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