A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203546



Internal ID21342361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20278025..20278025hg38UCSC Ensembl
chr7:20317648..20317648hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3952075
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203546
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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