A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146548



Internal ID21460421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36698050..36698050hg38UCSC Ensembl
chr7:36737655..36737655hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634583
Supporting Variants
SamplesHG02818
Known GenesAOAH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146548
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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