A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062765



Internal ID21433086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206524558..206524558hg38UCSC Ensembl
chr1:206697891..206697891hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618519
Supporting Variants
SamplesHG00731
Known GenesRASSF5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062765
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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