A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436477



Internal ID22494347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97507529..97507529hg38UCSC Ensembl
chr7:97136841..97136841hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436477
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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