A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15203400



Internal ID21342203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90344236..90344236hg38UCSC Ensembl
chr7:89973550..89973550hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3932871
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15203400
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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