A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150846



Internal ID21423675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97260908..97260908hg38UCSC Ensembl
chr6:97708784..97708784hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631950
Supporting Variants
SamplesHG00731
Known GenesMIR548H3, MMS22L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150846
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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