A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153952



Internal ID21406907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167997463..167997463hg38UCSC Ensembl
chr6:168398143..168398143hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382523
hg192523
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642781
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153952
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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