A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155259



Internal ID21425588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102378887..102378887hg38UCSC Ensembl
chr7:102019334..102019334hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640080
Supporting Variants
SamplesHG00731
Known GenesLOC100289561, LOC100630923
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155259
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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