A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148769



Internal ID21452792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:893603..893603hg38UCSC Ensembl
chr7:933240..933240hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633476
Supporting Variants
SamplesHG02011
Known GenesGET4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148769
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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