A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157239



Internal ID21512418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154496315..154496512hg38UCSC Ensembl
chr6:154817449..154817646hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5572450
Supporting Variants
SamplesNA24385
Known GenesCNKSR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157239
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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