A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147486



Internal ID21481117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40701895..40701895hg38UCSC Ensembl
chr7:40741494..40741494hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633957
Supporting Variants
SamplesHG03683
Known GenesC7orf10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147486
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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