A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150452



Internal ID21423484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136973069..136973069hg38UCSC Ensembl
chr7:136657816..136657816hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641198
Supporting Variants
SamplesHG00731
Known GenesCHRM2, LOC349160
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150452
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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