A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17157375



Internal ID21466940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2763191..2763191hg38UCSC Ensembl
chr7:2802825..2802825hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627300
Supporting Variants
SamplesHG03065
Known GenesGNA12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17157375
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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