A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203633



Internal ID21342438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73578776..73578776hg38UCSC Ensembl
chr7:72993106..72993106hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932300
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203633
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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