A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148331



Internal ID21446090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108025433..108025433hg38UCSC Ensembl
chr7:107665878..107665878hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634088
Supporting Variants
SamplesHG00732
Known GenesLAMB4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148331
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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