A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062086



Internal ID21432795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202205230..202205230hg38UCSC Ensembl
chr1:202174358..202174358hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620220
Supporting Variants
SamplesHG00731
Known GenesLGR6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062086
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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