A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427412



Internal ID22485282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1018714..1019074hg38UCSC Ensembl
chr6:1018949..1019309hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894287
Supporting Variants
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427412
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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