A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155806



Internal ID21473146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107686290..107686290hg38UCSC Ensembl
chr7:107326735..107326735hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642798
Supporting Variants
SamplesHG03371
Known GenesSLC26A4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155806
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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