A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433549



Internal ID22491419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98266507..98266811hg38UCSC Ensembl
chr7:97895819..97896123hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433549
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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