A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432868



Internal ID22490738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53861708..53861857hg38UCSC Ensembl
chr6:53726506..53726655hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5895753
Supporting Variants
Samples
Known GenesLRRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432868
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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