A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433101



Internal ID22490971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140481929..140490488hg38UCSC Ensembl
chr7:140181729..140190288hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg388560
hg198560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433101
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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