A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143842



Internal ID21409821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165301276..165301344hg38UCSC Ensembl
chr6:165714765..165714833hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575763
Supporting Variants
SamplesHG00512
Known GenesC6orf118
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143842
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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