A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445732



Internal ID22503602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27472344..27472596hg38UCSC Ensembl
chr6:27440123..27440375hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890407
Supporting Variants
Samples
Known GenesZNF184
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445732
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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